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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516968Generated: October 26, 2026

Chlorobenzene → 1-(4-(Bromomethyl)-2-chlorophenyl)ethanone

https://huagongshe.com/reaction/516968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(2-Chloro-4-methylphenyl)ethanoneHCID 15560949—
CatalystBenzoyl PeroxideHCID 7187—
SolventTolueneHCID 1140—
Product1-(4-(Bromomethyl)-2-chlorophenyl)ethanoneHCID 8985391470%

Reaction Conditions

Temperature142.5 °C

Reaction Steps

A mixture of 1-(2-chloro-4-methylphenyl)ethanone (1.6 g, 9.50 mmol) (preparation 15) and chlorobenzene (60 ml) was prepared at room temperature and N-bromosuccinimide (NBS) (1.86 g, 10.44 mmol) added followed by a catalytic amount of benzoyl peroxide (ca. 1.5 mg, 0.005 mmol), and the resulting mixture was heated to 140-145° C. for 16 h. The mixture was then allowed to cool to room temperature, diluted with toluene (50 ml) and filtered through a celite pad. The pad was washed with toluene (2×50 ml) and the filtrate concentrated under reduced pressure and purified by column chromatography (0-10% EtOAc/Hexanes) to afford 1-(4-(bromomethyl)-2-chlorophenyl)ethanone (1.65 g, 6.65 mmol, 70%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115088B2
Source datasetuspto-grants-2015_08
ORD IDord-63c8c2c23ef14ab3a813d19d099ced27
Source noteuspto-grants-2015_08