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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510829Generated: November 3, 2026

Benzoyl Peroxide → 1-[3-Bromo-4-(bromomethyl)-5-chloro-2-methoxyphenyl]ethanone

https://huagongshe.com/reaction/510829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(3-Bromo-5-chloro-2-methoxy-4-methylphenyl)ethanoneHCID 86666759—
SolventCarbon TetrachlorideHCID 5943—
Product1-[3-Bromo-4-(bromomethyl)-5-chloro-2-methoxyphenyl]ethanoneHCID 86666765—

Reaction Steps

A mixture of 1-(3-bromo-5-chloro-2-methoxy-4-methylphenyl)ethanone (3.3 g, 12 mmol), N-bromosuccinimide (2.2 g, 13 mmol), and benzoyl peroxide (0.15 g, 0.60 mmol) in carbon tetrachloride (50 mL) was heated at reflux overnight. The mixture was cooled to room temperature and concentrated. The resulting residue was diluted with ethyl acetate and washed with water. The organic layers were dried over magnesium sulfate and evaporated to dryness. The crude product was used directly in next step. LCMS calculated for C10H10Br2ClO2 (M+H)+: m/z=355.1. found: 355.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-fe69af24a12f4c9b90fea368797324c4
Source noteuspto-grants-2015_08