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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065577Generated: November 2, 2026

Benzoyl Peroxide → 3-(Bromomethyl)-2-chloro-1,1'-biphenyl

https://huagongshe.com/reaction/1065577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22013535HCID 22013535—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)-2-chloro-1,1'-biphenylHCID 2027063192.6%

Reaction Steps

A stirred solution of 2-chloro-3-methyl-[1,1'-biphenyl] (0.5 g, 0.0023 mole) in 8 ml of carbon tetrachloride was irradiated and heated to reflux with a 250 watt brooder lamp. A small amount of benzoyl peroxide was added and the reaction mixture refluxed for ten minutes. A second portion of benzoyl peroxide (total 0.01 g) was added, followed by N-bromosuccinimide (0.43 g, 0.0024 mole). The stirred reaction mixture was irradiated for 16 hours, then cooled, and then filtered. The filter cake was rinsed with carbon tetrachloride and the combined filtrates washed with aqueous saturated sodium chloride solution. The organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to give 3-bromomethyl-2-chloro-[1,1'-biphenyl] (0.6 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329518
Source datasetuspto-grants-1982_05
ORD IDord-1c15af0ff7444014af1dbb13d0d7b3d0
Source noteuspto-grants-1982_05