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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530815Generated: October 26, 2026

Sodium borohydride → 4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol

https://huagongshe.com/reaction/1530815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-(Benzyloxy)phenyl)-2,2,2-trifluoroethanoneHCID 21252691—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl AlcoholHCID 21252664—

Reaction Steps

At 20° C., a solution of 15.7 g of sodium borohydride in 100 ml of water was added dropwise with cooling to a solution of 72.5 g of 4′-benzyloxy-2,2,2-trifluoroacetophenone in 900 ml of ethanol. The mixture was stirred under reflux for 3 hours and then concentrated, the residue was taken up in diethyl ether and water and made slightly acidic using dilute hydrochloric acid, and the organic phase was dried and concentrated to give the title product as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197729B1
Source datasetuspto-grants-2001_03
ORD IDord-4a92d3c83db041b38275b9daed4ffa74
Source noteuspto-grants-2001_03