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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266023Generated: November 1, 2026

Epichlorohydrin → HCID 53710830, compound

https://huagongshe.com/reaction/266023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11016067HCID 11016067—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
ProductHCID 53710830HCID 5371083037%

Reaction Steps

A mixture of 50% NaOH (10 ml), epichlorohydrin (6 ml) and tetrabutylammonium hydrogen sulfate (0.3 g) kept at 0° C. was added drop by drop to a solution of (3α,5β,7α,12α)-3,7,12-trihydroxy-cholan-24-oic acid 1,1-dimethylethyl ester (prepared according to the procedure described by R. P. Bonar-Law et al., J. Chem. Soc. Perkin Trans. I, 1990, 2245) (0.0045 mol) in CH2Cl2 (10 ml). When the addition was completed the mixture was left to react at room temperature by 24 h. The organic phase was separated, washed with H2O to neutral, dried over Na2SO4 and evaporated. The residue was purified by flash chromatography to obtain 0.86 g of desired product (0.0017 mol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05649537
Source datasetuspto-grants-1997_07
ORD IDord-b83fdc54deb641d099b352f681b66431
Source noteuspto-grants-1997_07