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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714002Generated: November 1, 2026

Benzoyl Peroxide → 2-Bromo-5-chlorobenzyl bromide

https://huagongshe.com/reaction/1714002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-chlorotolueneHCID 84476—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-5-chlorobenzyl bromideHCID 1184650545%

Reaction Steps

1-bromo-2-(bromomethyl)-4-chlorobenzene was prepared according to literature precedent (J. Am. Chem. Soc. 2002, 124 (7), 1354): a suspension of 1-bromo-2-methyl-4-chlorobenzene (1 eq), NBS (1 eq) and benzoyl peroxide (0.004 eq) in CCl4 (0.7 M) was heated at reflux for 4 h. The reaction was then filtered whilst hot and the volatiles reduced in vacuo. PE was added, and the resultant precipitate filtered off and dried in vacuo to afford the title compound (45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795247B2
Source datasetuspto-grants-2010_09
ORD IDord-47a464bac5824b0a916dbf111ebfdf66
Source noteuspto-grants-2010_09