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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975212Generated: October 29, 2026

Water → 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanone

https://huagongshe.com/reaction/975212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,2,2-trifluoro-1-(3-methoxyphenyl)ethanolHCID 2829249—
ReactantSodium HypochloriteHCID 23665760—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product2,2,2-trifluoro-1-(3-methoxyphenyl)ethanoneHCID 2759734—

Reaction Steps

4.82 g (0.023 mol) of 2,2,2-trifluoro-1-(3-methoxyphenyl)ethanol and 0.4 g (0.0012 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 100 ml of methylene chloride at room temperature. 14.4 ml (0.028 mol) of an approximately 12% strength sodium hypochlorite solution are metered in within 15 minutes with vigorous stirring and the mixture is stirred for a further 6 hours during which the reaction temperature rises to 26° C. The reaction mixture is added to 100 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 (0.2 mbar, 60°-70° C. bath temperature), 2.1 g (44% of theory) of 3-trifluoroacetylanisole are obtained. nD20 : 1.4773.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608062
Source datasetuspto-grants-1997_03
ORD IDord-54638de163e34c6cb80914bf7378cad5
Source noteuspto-grants-1997_03