Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975218Generated: October 29, 2026

Water → 2,2,2-Trifluoroacetophenone

https://huagongshe.com/reaction/975218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(S)-alpha-(Trifluoromethyl)benzyl alcoholHCID 95556—
ReactantSodium HypochloriteHCID 23665760—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product2,2,2-TrifluoroacetophenoneHCID 9905—

Reaction Steps

10.0 g (0.057 mol) of 2,2,2-trifluoro-1-phenylethanol and 0.96 g (0.0028 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 250 ml of methylene chloride at room temperature. 35 ml (0.068 mol) of an approximately 12% strength sodium hypochlorite solution are metered in within 20 minutes with vigorous stirring and the mixture is stirred for a further 6 hours at room temperature. The reaction mixture is added to 200 ml of water, the phases are separated, the aqueous phase is extracted several times with methylene chloride and the combined organic phases are washed with saturated aqueous sodium chloride solution. After drying the organic phase with sodium sulfate, the volatiles are distilled off. Following distillation of the crude product in a kugelrohr (24 torr, 90°-115° C. bath temperature), 7.45 g (75% of theory) of trifluoroacetylbenzene are obtained. nD20 : 1.4658.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608062
Source datasetuspto-grants-1997_03
ORD IDord-1a18d78942494835add82f0922c806e9
Source noteuspto-grants-1997_03