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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063844Generated: November 3, 2026

Sodium Thiosulfate → 3-Bromo-4-fluorophenyl acetate

https://huagongshe.com/reaction/1063844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1-(3-Bromo-4-fluorophenyl)ethan-1-oneHCID 70508—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product3-Bromo-4-fluorophenyl acetateHCID 2078545968%

Reaction Steps

A solution of 1.09 gm (5 mMol) 3-bromo-4-fluoroacetophenone and 3.45 gm (20 mMol) m-chloroperbenzoic acid (70%) in 15 mL dichloromethane was heated at reflux for 18 hours. An additional 3.45 gm m-chloroperbenzoic acid were added and reflux continued for about 12 hours. At this point an additional 1.4 gm m-chloroperbenzoic acid were added and reflux continued for 18 hours. The reaction mixture was cooled to room temperature and was then diluted with 50 mL diethyl ether. The resulting mixture was cooled to 0° C. and was then treated with 15 mL 20% aqueous sodium thiosulfate. The resulting slurry was stirred for about 1 hour and then the phases separated. The organic phase was washed sequentially with 3×20 mL 20% aqueous sodium thiosulfate followed by 3×20 mL saturated aqueous sodium chloride. The organic phase was then dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 10:1 hexane:diethyl ether. Fractions containing product were combined and concentrated under reduced pressure to provide 68% of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967201B1
Source datasetuspto-grants-2005_11
ORD IDord-20d25e7c84c444d48820720d4fc56e88
Source noteuspto-grants-2005_11