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1 SUPPORTING INFORMATION Synthesis of long-chain polyols from the Claisen condensation of - valerolactone Camila S. Santos [a] , Caio Soares [b] , Adriano Siqueira [c] and Antonio C. B. Burtoloso* [a] Contents Page Derivatization of compound 3 2-3 1 H and 13 C NMR spectra of all products 5-36 Electronic Supplementary Material (ESI) for Green Chemistry. This journal is © The Royal Society of Chemistry 2019

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Page 1: SUPPORTING INFORMATION Synthesis of long …1 SUPPORTING INFORMATION Synthesis of long-chain polyols from the Claisen condensation of -valerolactone Camila S. Santos[a], Caio Soares[b],

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SUPPORTING INFORMATION

Synthesis of long-chain polyols from the Claisen condensation of -valerolactone

Camila S. Santos[a], Caio Soares[b], Adriano Siqueira[c] and Antonio C. B. Burtoloso*[a]

Contents Page

Derivatization of compound 3 2-3

1H and 13C NMR spectra of all products 5-36

Electronic Supplementary Material (ESI) for Green Chemistry.This journal is © The Royal Society of Chemistry 2019

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Derivatization of compound 3 for GC-MS analysis

Compound 3 (5 mg, 0,024 mmol), 0.5 mL of dry 2 Methyltetrahydrofuranand and 200 µL

of N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) were added to a 25 mL round

bottom flask. Next, the reaction was heated at 60°C during 2h. The system was cooled

to 25 °C and a 100 µL aliquot of the reaction medium was diluted in 5 mL of

dichloromethane. An aliquot of this solution was filtered off (Chromafil, Macherey-

Nagel, pore size 0.45μm) and injected into GC-MS. GC-MS analyses were carried out on

Shimadzu-CGMS QP 2010 ULTRA gas chromatography on RESTEK Rtx-5MS

5%diphenyl/95% dimethyl polysiloxane capillary Column 30 m × 0.25 mm, 0.25 μm, split

injector, entrained gas flow (He) 1.33 mL/min, injector 300 °C, interface 330 °C. Column

temperature was started from 45 °C maintained for 1 minute and increased to 170 °C

at the rate of 10 °C/min, remaining constant for 3 mim. Then, was heated to 330 °C at

the rate of 10 °C/min.

Figure 2. GC-MS chromatogram of silylated compound 3.

A)

B)

m/z= 247 (M+ - 247)

m/z= 247 (M+ - 247)

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Figure 3. Fragmentation of peaks with retention time A) 20.213, B) 20.280, C) 20.354, D)20.403.

C)

D)

m/z= 247 (M+ - 247)

m/z= 247 (M+ - 247)

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture

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Diastereisomeric mixture