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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824970Generated: October 30, 2026

Sodium borohydride → 3-(5-Trifluoromethylbenzofur-7-yl)-2-butanol

https://huagongshe.com/reaction/1824970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(5-Trifluoromethylbenzofur-7-yl)-2-butanoneHCID 22144922—
SolventEthanolHCID 702—
Product3-(5-Trifluoromethylbenzofur-7-yl)-2-butanolHCID 2214486445.4%

Reaction Steps

A solution of 0.09 gm (0.35 mMol) 3-(5-trifluoromethylbenzofur-7-yl)-2-butanone in ethanol was cooled to 0° C. To this solution was added 0.013 gm (0.35 mMol) sodium borohydride and the resulting mixture stirred for 30 minutes. The reaction mixture was then allowed to warm to room temperature and was concentrated under reduced pressure. The residue was taken up in ethyl acetate and washed sequentially with 0.1 N hydrochloric acid, water, and saturated aqueous sodium chloride. The remaining organic phase was concentrated under reduced pressure and the residue subjected to silica gel chromatography, eluting with 30% ethyl acetate in hexane. Fractions containing product were combined and concentrated under reduced pressure to provide 0.041 gm (45%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045545B1
Source datasetuspto-grants-2006_05
ORD IDord-5d44e87683e240ccb6b7652de52247e5
Source noteuspto-grants-2006_05