si tx-com-03-2014-000019.r1 proofs · 4 5-(hydroxymethyl)furfural, hmf (1)1 to a round-bottom flask...
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![Page 1: SI TX-COM-03-2014-000019.R1 proofs · 4 5-(Hydroxymethyl)furfural, HMF (1)1 To a round-bottom flask D-fructose (6 g, 33.3 mmol) and DMSO (200 mL) were added followed by the addition](https://reader034.vdocuments.site/reader034/viewer/2022050510/5f9ad1d2b398c543186a3177/html5/thumbnails/1.jpg)
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Supplementary Information
Emerging Platform from Renewable Resources: Selection Guidelines for Human
Exposure of Furfural‐related Compounds
Raquel F. M. Frade*,a, Jaime A. S. Coelhoa, Svilen P. Simeonova, Carlos A. M. Afonso*,a
a Instituto de Investigação do Medicamento (iMed.ULisboa), Faculty of Pharmacy, University of Lisbon, Av. Prof. Gama Pinto, 1649-003, Lisboa, Portugal
Procedures 3 5-(Hydroxymethyl)furfural, HMF (1) ................................................................................................................................... 4 Sodium (5-formylfuran-2-yl)methyl sulfate (2) .................................................................................................................... 4 5-(Chloromethyl)furan-2-carbaldehyde (3) .......................................................................................................................... 5 5-(Ethoxymethyl)furan-2-carbaldehyde (4) .......................................................................................................................... 5 5-((Benzyloxy)methyl)furan-2-carbaldehyde (5).................................................................................................................. 6 5-(((tert-Butyldimethylsilyl)oxy)methyl)furan-2-carbaldehyde (6) ...................................................................................... 6 (5-Formylfuran-2-yl)methyl acetate (7) ................................................................................................................................ 7 (5-Formylfuran-2-yl)methyl hexanoate (8) ........................................................................................................................... 7 (5-Formylfuran-2-yl)methyl benzoate (9) ............................................................................................................................. 8 Furan-2,5-dicarbaldehyde (10) ............................................................................................................................................. 8 Furan-2-carbaldehyde (11) ................................................................................................................................................... 9 Furan-2,5-diyldimethanol (12) .............................................................................................................................................. 9 (5-(Ethoxymethyl)furan-2-yl)methanol (13) ......................................................................................................................... 9 Sodium 5-(hydroxymethyl)furan-2-carboxylate (14) ......................................................................................................... 10 Furan-2-ylmethanol (15) ..................................................................................................................................................... 10 2,5-Bis(ethoxymethyl)furan (16) ........................................................................................................................................ 10 Furan-2,5-dicarboxylic acid, FDCA (17) ............................................................................................................................ 11 2,5-Dimethylfuran (18) ....................................................................................................................................................... 11 2-Methylfuran (19) ............................................................................................................................................................. 11 (5,5'-(Oxybis(methylene))bis(furan-5,2-diyl))dimethanol (20) .......................................................................................... 11 (5,5'-((1E,1'E)-hydrazine-1,2-diylidenebis(methanylylidene))bis(furan-5,2-diyl))dimethanol (21) ................................... 12 4-Oxopentanoic acid, levulinic acid (22) ............................................................................................................................ 12 Figures (HPLC, GC-MS and NMR) 13 Figure 1. HPLC chromatogram of 1. .................................................................................................................................. 13 Figure 2. HPLC chromatogram of 2. .................................................................................................................................. 13 Figure 3. HPLC chromatogram of 3. .................................................................................................................................. 14 Figure 4. HPLC chromatogram of 4. .................................................................................................................................. 14 Figure 5. HPLC chromatogram of 5. .................................................................................................................................. 15 Figure 6. HPLC chromatogram of 6. .................................................................................................................................. 15 Figure 7. HPLC chromatogram of 7. .................................................................................................................................. 16 Figure 8. HPLC chromatogram of 8. .................................................................................................................................. 16 Figure 9. HPLC chromatogram of 9. .................................................................................................................................. 17 Figure 10. HPLC chromatogram of 10. .............................................................................................................................. 17
Electronic Supplementary Material (ESI) for Toxicology Research.This journal is © The Royal Society of Chemistry 2014
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Figure 11. HPLC chromatogram of 11. .............................................................................................................................. 18 Figure 12. HPLC chromatogram of 13. .............................................................................................................................. 18 Figure 13. HPLC chromatogram of 16. .............................................................................................................................. 19 Figure 14. HPLC chromatogram of 17. .............................................................................................................................. 19 Figure 15. HPLC chromatogram of 18. .............................................................................................................................. 20 Figure 16. HPLC chromatogram of 19. .............................................................................................................................. 20 Figure 17. HPLC chromatogram of 20. .............................................................................................................................. 21 Figure 18. GC-MS chromatogram and MS of major signal of 1. ....................................................................................... 22 Figure 19. GC-MS chromatogram and MS of major signal of 3. ....................................................................................... 22 Figure 20. GC-MS chromatogram and MS of major signal of 6. ....................................................................................... 23 Figure 21. GC-MS chromatogram and MS of major signal of 7. ....................................................................................... 24 Figure 22. GC-MS chromatogram and MS of major signal of 11. ..................................................................................... 25 Figure 23. GC-MS chromatogram and MS of major signal of 12. ..................................................................................... 25 Figure 24. GC-MS chromatogram and MS of major signal of 15. ..................................................................................... 26 Figure 25. GC-MS chromatogram and MS of the major signals of 18. .............................................................................. 27 Figure 26. GC-MS chromatogram and MS of the major signals of 19. .............................................................................. 28 Figure 27. 1H NMR spectrum of 1. ..................................................................................................................................... 29 Figure 28. 13C NMR spectrum of 1. .................................................................................................................................... 30 Figure 29. 1H NMR spectrum of 2. ..................................................................................................................................... 31 Figure 30. 13C NMR spectrum of 2. .................................................................................................................................... 32 Figure 31. 1H NMR spectrum of 3. ..................................................................................................................................... 33 Figure 32. 1H NMR spectrum of 4. ..................................................................................................................................... 34 Figure 33. 13C NMR spectrum of 4. .................................................................................................................................... 35 Figure 34. 1H NMR spectrum of 5. ..................................................................................................................................... 36 Figure 35. 13C NMR spectrum of 5. .................................................................................................................................... 37 Figure 36. 1H NMR spectrum of 6. ..................................................................................................................................... 38 Figure 37. 13C NMR spectrum of 6. .................................................................................................................................... 39 Figure 38. 1H NMR spectrum of 7. ..................................................................................................................................... 40 Figure 39. 13C NMR spectrum of 7. .................................................................................................................................... 41 Figure 40. 1H NMR spectrum of 8. ..................................................................................................................................... 42 Figure 41. 13C NMR spectrum of 8. .................................................................................................................................... 43 Figure 42. 1H NMR spectrum of 9. ..................................................................................................................................... 44 Figure 43. 1H NMR spectrum of 10. ................................................................................................................................... 45 Figure 44. 13C NMR spectrum of 10. .................................................................................................................................. 46 Figure 45. 1H NMR spectrum of 12. ................................................................................................................................... 47 Figure 46. 13C NMR spectrum of 12. .................................................................................................................................. 48 Figure 47. 1H NMR spectrum of 13. ................................................................................................................................... 49 Figure 48. 1H NMR spectrum of 16. ................................................................................................................................... 50 Figure 49. 1H NMR spectrum of 17. ................................................................................................................................... 51 Figure 50. 1H NMR spectrum of 20. ................................................................................................................................... 52 Figure 51. 13C NMR spectrum of 20. .................................................................................................................................. 53 Figure 52. 1H NMR spectrum of 21. ................................................................................................................................... 54 Figure 53. 13C NMR spectrum of 21. .................................................................................................................................. 55 Toxicity curves 56 References 67
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Procedures General Remarks
All solvents were freshly distilled from commercial grade sources. Commercially available reagents were
used as received without further purification otherwise notice. Preparative thin-layer chromatography plate
was prepared with silica gel 60 GF254 MercK (ref 1.07730.1000), whereas flash chromatography was carried
out on silica gel 60M purchased from MN (Ref. 815381). Reaction mixtures were analyzed by TLC using
ALUGRAM SIL G/UV254 from MN (Ref. 818133, silica gel 60), and visualization by UV and
phosphomolybdic acid stain.
HPLC analysis was performed on Dionex P680 pump, Dionex UVD 340S diode array detector, detection
at 275 and 225 nm, manual injector with 20 μL loop, column HICHROM C18, 250x4.6mm, or Kromasil 100,
C18, 250x4.6mm. Mobile phase gradient from 1:99 to 50:50 for 40 min acetonitrile:water, and then 50:50 for
the time indicated in the chromatogram, flow 1 mL/min, The HPLC purity was determined by comparing the
integration area of the main signal with other observed minor peaks and are represented in the chromatograms
by relative area. Retention times were determined by using the mobile phase gradient from 1:99 to 90:10 in 50
min.
GC–MS analyses were performed on Gas Chromatograph Mass Spectrometer-QP2010S, Shimadzu by
using the column TRB-5MS-Teknokroma (30 m × 0.25 mm × 0.25 µm). GC program: column oven Tinitial=:
50.0 °C, Tfinal=: 250.0 °C, slope = 5ºC/min ; injection temperature: 250 °C; pressure: 77.9 kPa, total flow: 17.7
mL/min; column flow: 1.34 mL/min; linear velocity: 42.0 cm/sec; purge flow: 3.0 mL/min split ratio: 10.0,
high press. inj. pressure: 100.0 kPa, high press. inj. time: 1.00 min. MS program: start time: 3.00 min; end
time: 50.00 min; event time: 0.50 s; scan speed: 666; start: m/z = 40.00; end: m/z = 350.00.
NMR spectra were recorded at room temperature in a Bruker AMX 300 or Bruker AMX 400 using CDCl3,
D2O or DMSO-d6 as solvents and (CH3)4Si(1H) as internal standard.
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5-(Hydroxymethyl)furfural, HMF (1)1
To a round-bottom flask D-fructose (6 g, 33.3 mmol) and DMSO (200 mL) were added followed by the
addition of Amberlyst-15-powder (0.4 g, 15% w/w). The reaction was allowed to stir for 120 minutes at 120
ºC under inert atmosphere. After reaction the DMSO was removed by distillation and the crude reaction
mixture was purified by column chromatography with silica gel (hexane/ethyl acetate 1:1) to yield the product
(2.9 g, 70% yield) as a pale yellow oil that crystalizes in the freezer (0ºC). 1H NMR (300 MHz, CDCl3) δ 2.59
(s, 1H), 4.71 (s, 2H), 6.51 (d, J = 3.5 Hz, 1H), 7.21 (d, J = 3.5 Hz, 1H), 9.58 (s, 1H); 13C NMR (100 MHz,
CDCl3) δ 57.7, 110.1, 123.1, 152.4, 160.8, 177.9.
As alternative, HMF was synthetized using the recently reported protocol from our group, using
tetraethylammonium bromide and Amberlyst-15.2
Sodium (5-formylfuran-2-yl)methyl sulfate (2)3
To a solution of N,N'-Dicyclohexylcarbodiimide (1.0 g, 5 mmol) in DMF (3 mL) at 0 ºC, HMF (128 mg, 1
mmol) dissolved in DMF (0.5 mL) was added with vigorous stirring. A cold solution of sulfuric acid (2 mmol)
in DMF (1 mL) was added. The mixture was allowed to stir at 0 ºC for 1h. The mixture was then centrifuged
and the solution neutralized with methanolic NaOH 1M. The resulting solution was once again centrifuged.
The precipitate was washed with DMF and centrifuged. The collected organic phases were concentrated under
vacuum and the crude dissolved in ethanol and centrifuged. To the solution 10 volumes of Et2O was slowly
added and the precipitate centrifuged. The precipitate was then washed with Et2O to give the product as a pale
orange solid (55 mg, 24% yield); mp 128 ºC.
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5-(Chloromethyl)furan-2-carbaldehyde (3)4
OH
O
Cl
To a flame dried round bottom flask, HMF (1 g, 7.9 mmol) and CHCl3 were added. Trimethylsilyl chloride
(6 mL, 47.3 mmol, 6 equiv.) was added dropwise at 45 ºC and the resulting mixture stirred for 24 h at 45ºC
under inert atmosphere. The mixture was then quenched with saturated aqueous solution of NaHCO3 and
extracted with DCM. The collected organic layers were dried over Na2SO4 and the solvent removed. The
crude product was purified by dissolution in hot hexane and filtration through a pad of celite and activated
carbon. The hexane was removed under vacuum to give the desired product (0.7 g, 61% yield). 1H NMR (300
MHz, CDCl3) δ 4.59 (s, 2H), 6.57 (d, J = 3.57 Hz, 1H), 7.19 (d, J = 3.57 Hz, 1H), 9.60 (s, 1H).
5-(Ethoxymethyl)furan-2-carbaldehyde (4)5
HMF (1.0 g, 8.0 mmol) was dissolved in absolute EtOH (15 mL) then 3 drops of concentrated H2SO4 were
added and mixture was stirred for 5 h at reflux temperature. The reaction mixture was neutralized with
aqueous saturated solution of NaHCO3 and extracted with EtOAc. The organic phase was dried with MgSO4
and evaporated. The product was purified by silica flash chromatography using EtOAc/Hexane to give 703
mg (57% yield) of the desired product. 1H NMR (300 MHz, CDCl3) δ 1.20 (t, J = 7.0 Hz, 3H), 3.55 (q, J = 7
Hz, 2H), 4.49 (s, 2H), 6.49 (d, J = 3.52 Hz, 1H), 7.18 (d, J = 3.52 Hz, 1H), 9.56 (s, 1H); 13C NMR (100 MHz,
CDCl3) δ 15.1, 64.8, 66.7, 111.1, 152.6, 158.8, 177.9.
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5-((Benzyloxy)methyl)furan-2-carbaldehyde (5)6
Benzyl bromide (3.8 g, 22.2 mmol) and silver oxide (2.6 g, 11.1 mmol) were successively added to a
stirred solution of HMF (1.4 g, 11.1 mmol) dissolved in DMF (15 mL). The mixture was stirred for 50 h at
RT. The solution was evaporated under reduced pressure and the residue was chromatographed (silica;
hexane-EtOAc, 1:1) to give the desired product (1.2 g, 50 % yield). 1H NMR (300 MHz, CDCl3) δ 0.87 (t, J =
6.9 Hz, 3H), 1.27-1.31 (m, 4H), 1.63 (quint, J = 7.4 Hz, 2H), 2.35 (t, J = 7.6, 2H), 5.12 (s, 2H), 6.58 (d, J =
3.55 Hz, 1H), 7.21 (d, J = 3.55 Hz, 1H), 9.63 (s, 1H); 13C NMR (100 MHz, CDCl3) δ 64.2, 73.0, 111.4, 122.0,
128.0, 128.1, 128.6, 137.3, 152.7, 158.5, 177.8.
5-(((tert-Butyldimethylsilyl)oxy)methyl)furan-2-carbaldehyde (6)7
To a solution of HMF (1.6 g, 12.7 mmol) in DMF (3.2 mL) were added imidazole (2.2 g, 31.7 mmol, 2.5
equiv.) and tert-butyldimethylsilyl chloride (2.3 g, 15.2 mmol, 1.2 equiv.). The solution was stirred for 22 h.
The silylated compound was extracted with hexane (5 x 20 mL). The collected organic layers were washed
with brine, dried over Na2SO4, and the solvent removed to give the crude product that was distillated
(100ºC/0.8 mbar) giving the product (1.9 g, 63 % yield) as a light yellow liquid that solidifies in the freezer
(0ºC). 1H NMR (300 MHz, CDCl3) δ 0.08 (s, 6H), 0.89 (s, 9H), 4.71 (s, 2H), 6.45 (d, J = 3.53 Hz, 1H), 7.19
(d, J = 3.53 Hz, 1H), 9.56 (s, 1H); 13C NMR (100 MHz, CDCl3) δ -5.3, 18.4, 25.8, 58.7, 109.5, 122.6, 152.3,
161.5, 175.6.
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(5-Formylfuran-2-yl)methyl acetate (7)6
To a flame dried round-bottom flask, HMF (3.5 g, 27.8 mmol), MeCN (50 mL) and acetic anhydride (4.3
mL, 45.6 mmol) were added followed by catalytic amount of pyridine (0.5 mL, 6.2 mmol). The reaction
mixture was allowed to stir at room temperature for 22h under argon atmosphere. The solvent was removed
and the product purified by column chromatography with silica gel (hexane/ethyl acetate 8:2) to give the
product (4.3 g, 93% yield) as a pale yellow oil that crystallized in the freezer (0ºC). 1H NMR (300 MHz,
CDCl3) δ 2.11 (s, 3H), 5.12 (s, 2H), 6.58 (d, J = 3.55 Hz, 1H), 7.21 (d, J = 3.55 Hz, 1H), 9.64 (s, 1H); 13C
NMR (100 MHz, CDCl3) δ 20.8, 57.9, 112.7, 121.8, 153.0, 155.6, 170.5, 178.0.
(5-Formylfuran-2-yl)methyl hexanoate (8)8
To a flame dried round-bottom flask, HMF (0.250 g, 1.98 mmol), MeCN (10 mL) and hexanoic anhydride
(0.51 mL, 2.2 mmol, 1.1 equiv.) were added followed by catalytic amount of pyridine (32 µL, 0.4 mmol, 0.2
equiv.). The reaction mixture was allowed to stir at room temperature for 66 h under argon atmosphere. The
mixture was quenched with cold water, acidified with HCl 1M and extracted with Et2O. The combined
organic layers were dried over MgSO4, filtered and the solvent removed to give the crude product that was
purified by column chromatography with silica gel (hexane/ethyl acetate 8:2) to give the product (0.315 g,
71% yield) as a pale yellow oil. 1H NMR (300 MHz, CDCl3) δ 0.87 (t, J = 6.9 Hz, 3H), 1.27-1.31 (m, 4H),
1.63 (quint, J = 7.4 Hz, 2H), 2.35 (t, J = 7.6, 2H), 5.12 (s, 2H), 6.58 (d, J = 3.55 Hz, 1H), 7.21 (d, J = 3.55 Hz,
1H), 9.63 (s, 1H); 13C NMR (100 MHz, CDCl3) δ 14.0, 22.4, 24.6, 31.3, 34.06, 57.8, 112.6, 121.9, 152.9,
155.8, 173.3, 178.0.
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(5-Formylfuran-2-yl)methyl benzoate (9)9
To a flame dried round-bottom flask, HMF (1.0 g, 7.9 mmol) and pyridine (4 mL) were added followed by
benzoyl chloride (1 mL, 8.7 mmol, 1.1 equiv.). The reaction mixture was allowed to stir at reflux for 1.5 h
under argon atmosphere. The mixture was quenched with cold water (50 mL), acidified with HCl 1M and
extracted with Et2O. The combined organic layers were dried over MgSO4, filtered and the solvent removed
to give the crude product that was recrystallized from Et2O/hexane as a pale orange solid (0.86 g, 47% yield). 1H NMR (300 MHz, CDCl3) δ 5.38 (s, 2H), 6.68 (d, J = 3.55 Hz, 1H), 7.24 (d, J = 3.55 Hz, 1H), 7.46 (t, J =
7.7 Hz, 2H), 7.58 (tt, J = 7.45, 1.30 Hz, 1H), 8.06 (m, 2H), 9.65 (s, 1H).
Furan-2,5-dicarbaldehyde (10)10
To a flame dried schlenk with CH2Cl2 (100 mL) at -78ºC under argon atmosphere oxalyl chloride (0.85
mL, 1.25 equiv.) was added followed by dropwise addition of DMSO (1.13 mL, 2 equiv.). After stirring for 15
minutes, a solution of HMF (1.0 g, 8.0 mmol) in CH2Cl2 (10 mL) was added dropwise and the resulting
mixture was stirred at -78ºC for an additional 30 minutes. Et3N was then added dropwise and the mixture was
allowed to warm up to RT. After 1 hour of stirring at RT, water (50 mL) was added and the resulting mixture
was washed with HCl 1M, extracted with CH2Cl2 and finally dried over Na2SO4. The resulting crude mixture
was purified by flash chromatography with Et2O/Hexane. The collected solid was further recrystallized from
hexane/EtOAc to give 305 mg (31% yield) of the product as white needles. 1H NMR (300 MHz, CDCl3) δ 7.3
(s, 2H), 9.86 (s, 2H); 13C NMR (100 MHz, CDCl3) δ 119.4, 154.4, 179.4.
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Furan-2-carbaldehyde (11)
The commercial available compound was purified by distillation under vacuum to give a colorless oil.
Furan-2,5-diyldimethanol (12)11
To a solution of HMF (2g, 16mmol) in dry THF (10 mL), NaBH4 (2.4g, 64 mmol) was added portionwise.
The reaction mixture was stirred at RT overnight. MeOH (7 mL) and acetic acid (9 mL) were added and
stirred at RT for 15 min then 50 mL of MeOH was added and the solvent removed under vacuum. Then twice
50 ml MeOH were added and evaporated. The mixture was dissolved in DCM/MeOH 9:1 and passed through
a pad of silica gel. The solvent was evaporated and the product was purified by silica flash chromatography
using EtOAc/Hexane to give 1.6g (80% yield) of the product. 1H NMR (300 MHz, D2O) δ 4.51 (s, 4H), 6.31
(s, 2H); 13C NMR (100 MHz, D2O) δ 55.8, 109.0, 153.6.
(5-(Ethoxymethyl)furan-2-yl)methanol (13)12
5-(ethoxymethyl)furan-2-carbaldehyde (154 mg, 1 mmol) were dissolved in MeOH (5 mL) then NaBH4
(148mg, 4 mmol) was added on 3 portions at RT. The reaction mixture was stirred for 15 min and quenched
with H2O. The MeOH was evaporated and the water phase extracted with EtOAc. The organic phase was
dried with MgSO4 and evaporated. The product was purified by silica flash chromatography using
EtOAc/Hexane to give 148mg (95% yield) of the title compound. 1H NMR (300 MHz, CDCl3) δ 1.19 (t, J =
7.0 Hz, 3H), 2.62-2.74 (b, 1H), 3.51 (q, J = 7 Hz, 2H), 4.39 (s, 2H), 6.53 (s, 2H), 6.20 (m, 1H), 6.23 (m, 1H).
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Sodium 5-(hydroxymethyl)furan-2-carboxylate (14)13
To a closed vessel containing a solution of HMF (3 g, 24 mmol) in water (30 mL), NaOH (0.87 g, 22
mmol) was added at 0ºC, and the resulting mixture stirred for 18h at 0 ºC. The water was removed under
vacuum and ethyl acetate (2 x 50 mL) was added to the solid residue to separate the furan-2,5-diyldimethanol
(0.85g, 30% yield). From the remaining solid, the title compound was isolated by recrystallization with
ethanol (2 mL)/ethyl acetate (100 mL) to give the product as a hygroscopic solid (1.4 g, 41% yield). 1H NMR
(400MHz, D2O): δ 6.90 (d, J = 3.3Hz, 1H), 6.43 (d, J = 3.3Hz, 1H), 4.54 (s, 2H); 13C NMR (100 MHz, D2O):
δ 166.5, 155.6, 149.0, 115.7, 109.9, 55.9; ESI (-) MS: m/z 140.89.
Furan-2-ylmethanol (15)
The commercial available compound was purified by distillation under vacuum to give a colorless oil.
2,5-Bis(ethoxymethyl)furan (16)12
(5-(ethoxymethyl)furan-2-yl)methanol (390mg, 2.5mmol) was dissolved in acetonitrile (5 mL) then NaH
(0.2g, 8.3mmol) was added followed by dropwise addition of bromoethane (0.6 mL, 8 mmol). The reaction
mixture was stirred at RT overnight. The reaction was quenched with H2O and the acetonitrile was evaporated
and the water phase extracted with Et2O. The organic phase was dried with MgSO4 and evaporated. The
product was purified by silica flash chromatography using EtOAc/Hexane to give 180 mg (39%) of the
desired product. 1H NMR (300 MHz, CDCl3) δ 1.20 (t, J = 7.0 Hz, 6H), 3.52 (q, J = 7 Hz, 4H), 4.41 (s, 4H),
6.24 (s, 2H).
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Furan-2,5-dicarboxylic acid, FDCA (17)14
To a solution of sodium hydroxide (958 mg, 23 mmol) in water (10 mL), HMF (126 mg, 1 mmol) was
added at 20 ºC, followed by the addition of potassium permanganate (363 mg, 2.3 mmol). After 10 minutes
stirring at 20ºC the precipitate was filtered off and a concentrated HCl solution was added to the filtrate until
pH 1. The resulted precipitate was separated by filtration, washed with water and dried under vacuum to give
FDCA (106 mg, 68% yield) as a white powder. 1H NMR (300 MHz, D2O) δ 7.25 (s).
2,5-Dimethylfuran (18)
The commercial available source was used as received.
2-Methylfuran (19)
The commercial available source was used as received.
(5,5'-(Oxybis(methylene))bis(furan-5,2-diyl))dimethanol (20)15
The title compound was isolated by silica gel column chromatography EtOAc/Hexane as a 10% side
product from the following reaction. To 9.1g of Et4NBr (1% water content w/w) was mixed with 2g of
fructose and 0.2g of smashed Amberlyst-15® (10% w/w). The mixture was placed at 80 ˚C and heated up to
100 ˚C for 10 min. Then the mixture was stirred at 100 ˚C for 30 min. The mixture was cooled down to RT
and the resulting solid was washed with EtOAc (50 mL). The solvent was decanted and the solid was
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dissolved in hot EtOH (2 mL) then under vigorous stirring EtOAc (200 mL) was added. The resulting
precipitated was filtered out and the combined solutions were filtered through a pad of silica gel (10g) and
evaporated to give brown liquid of HMF (1.25g, 71%) in 88% purity by HPLC and 10% of the desire
compound which was isolated by silica flash chromatography, EtOAc/Hexane. 1H NMR (300 MHz, CDCl3) δ
4.63 (s, 4H), 6.57 (d, J = 3.55 Hz, 2H), 7.21 (d, J = 3.55 Hz, 2H), 9.63 (s, 2H); 13C NMR (100 MHz, CDCl3) δ
64.8, 112.0, 122.0, 152.9, 157.4, 177.9.
(5,5'-((1E,1'E)-hydrazine-1,2-diylidenebis(methanylylidene))bis(furan-5,2-diyl))dimethanol (21)16
HMF (1.0 g, 8.0 mmol) and hydrazine monohydrate (0.4 mL, 8.0 mmol) was dissolved in absolute EtOH
(15 mL) then 3 drops of concentrated H2SO4. The mixture was stirred at RT for 1h. The resulting solid was
filtered and washed with absolute EtOH to give the desired product 1.7 g (86% yield). 1H NMR (300 MHz,
DMSO-d6) δ 4.45 (s, 2H), 4.47 (s, 2H), 5.43 (t, 2H), 6.50 (s, 2H), 7.02 (s, 2H), 8.44 (s, 2H); 13C NMR (100
MHz, DMSO-d6) δ 55.8, 109.6, 118.4, 148.4, 150.2, 159.4.
4-Oxopentanoic acid, levulinic acid (22)
The commercial available source was used as received.
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HPLC
Figure 1. HPLC chromatogram of 1.
Figure 2. HPLC chromatogram of 2.
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Figure 3. HPLC chromatogram of 3.
Figure 4. HPLC chromatogram of 4.
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Figure 5. HPLC chromatogram of 5.
Figure 6. HPLC chromatogram of 6.
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Figure 7. HPLC chromatogram of 7.
Figure 8. HPLC chromatogram of 8.
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Figure 9. HPLC chromatogram of 9.
Figure 10. HPLC chromatogram of 10.
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Figure 11. HPLC chromatogram of 11.
Figure 12. HPLC chromatogram of 13.
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Figure 13. HPLC chromatogram of 16.
Figure 14. HPLC chromatogram of 17.
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Figure 15. HPLC chromatogram of 18.
Figure 16. HPLC chromatogram of 19.
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Figure 17. HPLC chromatogram of 20.
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GC-MS
Figure 18. GC-MS chromatogram and MS of major signal of 1.
Figure 19. GC-MS chromatogram and MS of major signal of 3.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.00.0
0.5
1.0
1.5
2.0
2.5
3.0
3.5
4.0
4.5
5.0
5.5(x100,000)
TIC
40 50 60 70 80 90 100 110 1200.0
25.0
50.0
75.0
100.0
%
41
97695153
1268144
10966 9862
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.0
0.00
0.25
0.50
0.75
1.00
1.25
(x10,000,000)TIC
40 50 60 70 80 90 100 110 120 130 140 1500.0
25.0
50.0
75.0
100.0
%
109
53144
81
146110
8749 7942 61 12411773 95
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Figure 20. GC-MS chromatogram and MS of major signal of 6.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.00.0
1.0
2.0
3.0
4.0
5.0(x10,000,000)
TIC
36.00 36.25 36.50 36.75 37.00 37.25 37.50 37.75 38.00
0.0
2.5
5.0
7.5
(x10,000,000)TIC
50.0 75.0 100.0 125.0 150.0 175.0 200.0 225.0 250.0 275.0 300.00.0
5.0
10.0
15.0
20.0
25.0
%
18311175
61 139
53 99
15541
121
225167 195 211 239 309
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Figure 21. GC-MS chromatogram and MS of major signal of 7.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.0
0.00
0.25
0.50
0.75
1.00
1.25
(x1,000,000)TIC
50.0 75.0 100.0 125.0 150.00
10
20
30
40
50
%43
126
53
79
41 109
6997
1259870 16861
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Figure 22. GC-MS chromatogram and MS of major signal of 11.
Figure 23. GC-MS chromatogram and MS of major signal of 12.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.0
0.0
1.0
2.0
3.0
(x10,000,000)TIC
4.5 5.0 5.5 6.0 6.5 7.0 7.5 8.0 8.5 9.0 9.5 10.0
0.0
0.5
1.0
1.5
2.0
(x10,000,000)TIC
40 50 60 70 80 90 1000.0
25.0
50.0
75.0
100.0
%
96
6740 42 5149 98656154 70 7977 93
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.0-0.25
0.00
0.25
0.50
0.75
1.00(x100,000)
TIC
40 50 60 70 80 90 100 110 120 1300.0
25.0
50.0
75.0
100.0
%
41 53
51
6997
4381
109
65 12883
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Figure 24. GC-MS chromatogram and MS of major signal of 15.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.0
0.0
1.0
2.0
3.0
(x10,000,000)TIC
4.5 5.0 5.5 6.0 6.5 7.0 7.5 8.0 8.5 9.0 9.5 10.0
0.0
1.0
2.0
3.0
(x10,000,000)TIC
50.0 75.0 100.0 125.0 150.00.0
25.0
50.0
75.0
100.0
%
98
41
8153
69
51
7961 91 160131103 148119
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Figure 25. GC-MS chromatogram and MS of the major signals of 18.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.00.25
0.50
0.75
1.00
1.25
1.50
1.75
2.00
(x100,000)TIC
40 50 60 70 80 90 100 1100.0
25.0
50.0
75.0
100.0
%
43
97
69
41 53 1125581 9884
40 50 60 70 80 90 100 1100.0
25.0
50.0
75.0
100.0
%
43
97
69112
41 5553 9870
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Figure 26. GC-MS chromatogram and MS of the major signals of 19.
5.0 10.0 15.0 20.0 25.0 30.0 35.0 40.0 45.00.25
0.50
0.75
1.00
1.25(x100,000)
TIC
40 50 60 70 80 90 1000.0
25.0
50.0
75.0
100.0
%
43
83 98
55
69
41 53 7081
40 50 60 70 80 90 1000.0
25.0
50.0
75.0
100.0
%
55
43 98
41
50.0 75.0 100.0 125.0 150.0 175.00.0
25.0
50.0
75.0
100.0
%
43
137
109
16281
180
91556541 119
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NMR Spectra
Figure 27. 1H NMR spectrum of 1.
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Figure 28. 13C NMR spectrum of 1.
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Figure 29. 1H NMR spectrum of 2.
2.22
1.07
1.00
1.13
1.87
4.54
4.79
6.42
6.43
6.90
6.90
8.41
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Figure 30. 13C NMR spectrum of 2.
55.8
6
109.
86
115.
73
148.
97
155.
60
166.
51
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Figure 31. 1H NMR spectrum of 3.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
140
150
160
170
180
190
6.56.66.76.86.97.07.17.27.3f1 (ppm)
0
10
20
30
1
2 3
4
O56
H7
O8
9
Cl10
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Figure 32. 1H NMR spectrum of 4.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
6.56.76.97.17.3f1 (ppm)
0
10
20
30
3.60f1 (ppm)
0
10
20
30
40
50
60
f1 (ppm)
0
50
100
150
1 2
3
O4
5
67
O8
O9
10CH311
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Figure 33. 13C NMR spectrum of 4.
-100102030405060708090110130150170190210f1 (ppm)
-30
-20
-10
0
10
20
30
40
50
60
70
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160
170
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210
220
1 2
3
O4
5
67
O8
O9
10CH311
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Figure 34. 1H NMR spectrum of 5.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
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90
100
110
120
130
140
150
1
2 3
4
O56
H7
O8
9
O10
11
12
13
1415
16
17
4.554.604.65f1 (ppm)
0
50
6.56.66.76.86.97.07.17.27.37.4f1 (ppm)
0
50
100
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Figure 35. 13C NMR spectrum of 5.
0102030405060708090100110120130140150160170180190200210f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
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110
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130
1
2 3
4
O56
H7
O8
9
O10
11
12
13
1415
16
17
128.0128.4128.8f1 (ppm)
0
50
100
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Figure 36. 1H NMR spectrum of 6.
-0.50.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.0f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
1
2 3
4
O56
H7
O8
9
O10
Si11
12
CH313
CH314
CH315
CH316CH3
17
6.46.56.66.76.86.97.07.17.27.3f1 (ppm)
0
2
4
6
8
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Figure 37. 13C NMR spectrum of 6.
-100102030405060708090100110120130140150160170180190200210f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
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1
2 3
4
O56
H7
O8
9
O10
Si11
12
CH313
CH314
CH315
CH316CH3
17
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Figure 38. 1H NMR spectrum of 7.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
50
60
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80
90
100
6.56.76.97.17.3f1 (ppm)
0
5
10
151
2 3
4
O56
H7
O8
9
O10
11
CH312
O13
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Figure 39. 13C NMR spectrum of 7.
-100102030405060708090110130150170190210f1 (ppm)
-4
-2
0
2
4
6
8
10
12
14
16
18
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26
28
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32
34
36
1
2 3
4
O56
H7
O8
9
O10
11
CH312
O13
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Figure 40. 1H NMR spectrum of 8.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.5f1 (ppm)
-10
0
10
20
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150
6.76.97.1f1 (ppm)
0
10
20
30
0.00.51.01.52.02.53.0f1 (ppm)
0
10
20
30
40
50
60
701
2 3
4
O56
H7
O8
9
O10
11
12
O13
14
1516
CH317
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43
Figure 41. 13C NMR spectrum of 8.
0102030405060708090100110120130140150160170180190200210f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
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1
2 3
4
O56
H7
O8
9
O10
11
12
O13
14
1516
CH317
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44
Figure 42. 1H NMR spectrum of 9.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
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100
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120
130
2.09
1.01
1.01
2.08
1.04
2.03
1.00
1.19
1.21
1.22
2.11
3.45
3.47
3.48
5.38
6.67
6.68
7.23
7.24
7.45
7.47
8.04
8.05
8.05
8.07
8.07
9.65
1
2 3
4
O56
H7
O8
9
O10
11
12
O13
14
1516
17
18
6.46.66.87.07.27.47.67.88.08.2f1 (ppm)
0
10
20
30
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45
Figure 43. 1H NMR spectrum of 10.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
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60
70
80
90
100
110
120
130
12
3
O4
56 7
H8
O9
H10
O11
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46
Figure 44. 13C NMR spectrum of 10.
-100102030405060708090110130150170190210f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
12
3
O4
56 7
H8
O9
H10
O11
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47
Figure 45. 1H NMR spectrum of 12.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
140
150
1
2 3
4
O56
OH7
8
OH9
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48
Figure 46. 13C NMR spectrum of 12.
0102030405060708090100110120130140150160170180190200f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
140
150
160
1
2 3
4
O56
OH7
8
OH9
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49
Figure 47. 1H NMR spectrum of 13.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.0f1 (ppm)
-100
0
100
200
300
400
500
600
700
800
900
1000
1100
1200
1300
1400
1500
1600
6.26.3f1 (ppm)
0
200
400
600
3.53.6f1 (ppm)
0
100
200
300
400
500
1.20f1 (ppm)
0
500
10001
O2
3
4 5
6
OH7
8
O9
10
CH311
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50
Figure 48. 1H NMR spectrum of 16.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
1
O2
3
4 5
6
O7
8
CH39
10
O11
12
CH313
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51
Figure 49. 1H NMR spectrum of 17.
0123456789101112131415f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
1
2 3
4
O56
OH7
O8
9
OH10
O11
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52
Figure 50. 1H NMR spectrum of 20.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
6.56.66.76.86.97.07.17.27.3f1 (ppm)
0
10
20
30 12
3O4
56
O7
8 9
1011
12
O1314
15
O16
O17
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53
Figure 51. 13C NMR spectrum of 20.
-100102030405060708090110130150170190210f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
120
130
12
3O4
56
O7
8 9
1011
12
O1314
15
O16
O17
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54
Figure 52. 1H NMR spectrum of 21.
0.00.51.01.52.02.53.03.54.04.55.05.56.06.57.07.58.08.59.09.510.5f1 (ppm)
-10
0
10
20
30
40
50
60
70
80
90
100
110
1 2
3
O4
56
OH7
8
N9
N10
11
12 13
14
O15
1617
OH18
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55
Figure 53. 13C NMR spectrum of 21.
-100102030405060708090110130150170190210f1 (ppm)
0
10
20
30
40
50
60
70
80
90
1 2
3
O4
56
OH7
8
N9
N10
11
12 13
14
O15
1617
OH18
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56
Toxicity curves
Compound 1
1.8 2.0 2.2 2.4 2.6 2.8 3.080
90
100
110
Log10(M)
Via
bil
ity
(%)
Compound 2
1.8 2.0 2.2 2.4 2.6 2.8 3.050
60
70
80
90
100
110
Log10(M)
Via
bil
ity
(%)
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57
Compound 3
1.8 2.0 2.2 2.4 2.6 2.8 3.050
60
70
80
90
100
110
Log10(M)
Via
bil
ity
(%)
Compound 4
1.8 2.0 2.2 2.4 2.6 2.8 3.060
80
100
120
140
Log10(M)
Via
bil
ity
(%)
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58
Compound 5
1.8 2.0 2.2 2.4 2.6 2.8 3.050
60
70
80
90
100
Log10(M)
Via
bil
ity
(%)
Compound 6
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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59
Compound 7
1.8 2.0 2.2 2.4 2.6 2.8 3.060
70
80
90
100
110
120
Log10(M)
Via
bil
ity
(%)
Compound 8
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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60
Compound 9
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
Compound 10
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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61
Compound 11
1.8 2.0 2.2 2.4 2.6 2.8 3.070
80
90
100
110
Log10(M)
Via
bil
ity
(%)
Compound 12
1.8 2.0 2.2 2.4 2.6 2.8 3.080
90
100
110
120
130
Log10(M)
Via
bil
ity
(%)
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62
Compound 13
1.8 2.0 2.2 2.4 2.6 2.8 3.080
90
100
110
120
130
140
Log10(M)
Via
bil
ity
(%)
Compound 14
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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Compound 15
1.8 2.0 2.2 2.4 2.6 2.8 3.070
80
90
100
110
120
Log10(M)
Via
bil
ity
(%)
Compound 16
1.8 2.0 2.2 2.4 2.6 2.8 3.060
80
100
120
140
Log10(M)
Via
bil
ity
(%)
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64
Compound 17
1.8 2.0 2.2 2.4 2.6 2.8 3.090
100
110
120
130
Log10(M)
Via
bil
ity
(%)
Compound 18
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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Compound 19
1.8 2.0 2.2 2.4 2.6 2.8 3.080
90
100
110
Log10(M)
Via
bil
ity
(%)
Compound 20
1.8 2.0 2.2 2.4 2.6 2.8 3.00
50
100
150
Log10(M)
Via
bil
ity
(%)
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Compound 21
1.8 2.0 2.2 2.4 2.6 2.8 3.080
90
100
110
120
130
Log10(M)
Via
bil
ity
(%)
Compound 22
1.8 2.0 2.2 2.4 2.6 2.8 3.085
90
95
100
105
110
115
Log10(M)
Via
bil
ity
(%)
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67
References
(1) Shimizu, K.; Uozumi, R.; Satsuma, A. Catal. Commun. 2009, 10, 1849. (2) Svilen, P.; Coelho, J. A. S.; Afonso, C. A. M. Chemsuschem 2012, 5, 1388. (3) Monien, B. H.; Frank, H.; Seidel, A.; Glattt, H. Chem. Res. Toxicol. 2009, 22, 1123. (4) Sanda, K.; Rigal, L.; Gaset, A. Carbohydr. Res. 1989, 187, 15. (5) Mascal, M.; Nikitin, E. B. Angewandte Chemie International Edition 2008, 47, 7924. (6) Cottier, L.; Descotes, G.; Eymard, L.; Rapp, K. Synthesis 1995, 303. (7) Cottier, L.; Descotes, G.; Soro, Y. J. Carbohyd. Chem. 2005, 24, 55. (8) Dai, H. L.; Shen, Q.; Zheng, J. B.; Li, J. Y.; Wen, R.; Li, J. Lett. Org. Chem. 2011, 8, 526. (9) Bognar, R.; Herczegh, P.; Zsely, M.; Batta, G. Carbohydr. Res. 1987, 164, 465. (10) Mehdi, H.; Bodor, A.; Lantos, D.; Horváth, I. T.; De Vos, D. E.; Binnemans, K. The Journal of
Organic Chemistry 2006, 72, 517. (11) Cottier, L.; Descotes, G. R.; Soro, Y. Synthetic. Commun. 2003, 33, 4285. (12) Balakrishnan, M.; Sacia, E. R.; Bell, A. T. Green Chemistry 2012, 14, 1626. (13) Gupta, N. K.; Nishimura, S.; Takagaki, A.; Ebitani, K. Green Chemistry 2011, 13, 824. (14) KAISHA, C. K., 2007. (15) Cottier, L.; Descotes, G.; Eymard, L.; Rapp, K. Synthesis 1995, 1995, 303. (16) Knotz, F. scientia pharmaceutica 1961, 29, 20.