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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749936Generated: October 30, 2026

Benzoyl Peroxide → 7-bromomethylbenzofuran-3(2H)-one

https://huagongshe.com/reaction/1749936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
Reactant7-Methylbenzofuran-3(2H)-oneHCID 12632—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product7-bromomethylbenzofuran-3(2H)-oneHCID 6015578949%

Reaction Steps

A solution of 7-methylbenzofuran-3(2H)-one (0.759 g, 5.12 mol) in carbon tetrachloride (50 mL) was added with N-bromosuccinimide (1.00 g, 5.63 mmol) and benzoyl peroxide (0.0830 g, 0.256 mmol), and the mixture was refluxed for 4 hours by heating. The reaction mixture was cooled to room temperature, and then filtered, and the resulting filtrate was concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain 7-bromomethylbenzofuran-3(2H)-one (0.573 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-86434c2654e24d37b65fccdd05a66b22
Source noteuspto-grants-2015_10