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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530816Generated: October 26, 2026

4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl Alcohol → 4-(2,2,2-Trifluoro-1-hydroxyethyl)phenol

https://huagongshe.com/reaction/1530816

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)-alpha-(trifluoromethyl)benzyl AlcoholHCID 21252664—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product4-(2,2,2-Trifluoro-1-hydroxyethyl)phenolHCID 11286977—

Reaction Steps

At 50° C. and a hydrogen pressure of 5 bar, 65.7 g (233 mmol) of 1-benzyloxy-4-(1-hydroxy-2,2,2-trifluoroethyl)benzene were hydrogenated in the presence of 5.2 g of palladium (10% on carbon) in 500 ml of glacial acetic acid. The catalyst was filtered off and the mixture was concentrated. This gave 44.1 g (99% of theory) of the product as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197729B1
Source datasetuspto-grants-2001_03
ORD IDord-166f643d580845d6bac7ff1b171f6f5c
Source noteuspto-grants-2001_03