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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909556Generated: October 25, 2026

Benzoyl chloride → 7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-one

https://huagongshe.com/reaction/1909556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-oneHCID 58566299—
SolventCarbon TetrachlorideHCID 5943—
Product7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-oneHCID 58566723—

Reaction Steps

A solution of provide 5-fluoro-2,2,7-trimethylbenzofuran-3(2H)-one (659) (100 mg, 0.515 mmol), N-Bromosuccinimide (100.8 mg, 0.567 mmol), benzoyl chloride (1.2 mg, 0.005 mmol) and carbon tetrachloride (2 mL) was heated at reflux overnight. Saturated sodium bicarbonate was added and extracted with ethyl acetate, dried over sodium sulfate, filtered and concentrated in vacuo. The crude compound was purified by flash column chromatography on silica gel with hexanes and EtOAc (5%) to give 7-(bromomethyl)-5-fluoro-2,2-dimethylbenzofuran-3(2H)-one (660).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598374B2
Source datasetuspto-grants-2013_12
ORD IDord-a020fb646b1a407b9ce4dda8b5fe42ad
Source noteuspto-grants-2013_12