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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975217Generated: October 29, 2026

Water → 2-Phenoxy-4-trifluoroacetylfluorobenzene

https://huagongshe.com/reaction/975217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 19971591HCID 19971591—
ReactantSodium HypochloriteHCID 23665760—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product2-Phenoxy-4-trifluoroacetylfluorobenzeneHCID 19971586—

Reaction Steps

14.37 g (0.05 mol) of 2,2,2-trifluoro-1-(4-fluoro-3-phenoxyphenyl)ethanol and 0.85 g (0.0025 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 200 ml of methylene chloride at room temperature. 31 ml (0.06 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 (0.2 mbar, 150°-165° C. bath temperature), 10.8 g (76% of theory) of 2-phenoxy-4-trifluoroacetylfluorobenzene are obtained. nD20 : 1.5230.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608062
Source datasetuspto-grants-1997_03
ORD IDord-b40a74212fbe442891043a75d060a2d9
Source noteuspto-grants-1997_03