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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975215Generated: October 30, 2026

Water → 1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethan-1-one

https://huagongshe.com/reaction/975215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodiumHCID 5360545—
Reactant1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethanolHCID 19971580—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventDichloromethaneHCID 6344—
Product1-(5-Bromothiophen-2-yl)-2,2,2-trifluoroethan-1-oneHCID 19971587—

Reaction Steps

2.93 g (0.011 mol) of 2,2,2-trifluoro-1-(5-bromo-2-thienyl)ethanol and 0.19 g (0.0006 mol) of tetrabutylammonium hydrogen sulfate are dissolved in 100 ml of methylene chloride at room temperature. 6.9 ml (0.014 mol) of an approximately 12% strength sodium hyochlorite solution are metered in within 5 minutes with vigorous stirring and the mixture is stirred for a further 4 hours at room temperature. 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 (0.3 mbar, 40°-60° C. bath temperature), 0.48 g (39% of theory) of 5-bromo-2-trifluoroacetylthiophene. nD20 : 1.5309.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608062
Source datasetuspto-grants-1997_03
ORD IDord-a14f8ecb6f7a40bb92f007a077454e5e
Source noteuspto-grants-1997_03