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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906838Generated: October 31, 2026

Benzoyl Peroxide → 4-Bromo-1-(bromomethyl)-2-chlorobenzene

https://huagongshe.com/reaction/906838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Bromo-2-chlorotolueneHCID 2735554—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-1-(bromomethyl)-2-chlorobenzeneHCID 2191448660%

Reaction Steps

4-Bromo-2-chloro-1-methyl-benzene (2.5 mL, 18.7 mmoles) and N-bromosuccinimide (4.0 g, 22.5 mmoles) were dissolved into 50 mL of CCl4. To this stirring mix was added benzoyl peroxide (0.5 g, 2.1 mmoles) and the solution was irradiated using white light. Enough light intensity was utilized to affect gentle reflux for 2 hours. After this period the mixture was cooled to ambient temperature and benzoyl peroxide (0.5 g, 2.1 mmoles) was added. Again, the mix was irradiated to reflux for a period of 2 hours. After this period the reaction mix was chilled to ambient temperature and was gravity filtered. The filtrate was evaporated in vacuo and the resulting crude residue was purified using flash silica chromatography (0-1% EtOAc/Hexane) to yield 4-bromo-1-bromomethyl-2-chloro-benzene (3.04 g, 60%) as a clear liquid. 1H-NMR (CDCl3): δ 7.57 (d, J=2.0 Hz, 1H), 7.39 (dd, J′=8.3 Hz, J″=1.8 Hz, 1H), 7.31 (d, J=8.1 Hz, 1H), 4.53 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013001B2
Source datasetuspto-grants-2011_09
ORD IDord-9eb9da79362c4ec982af333101cd6aeb
Source noteuspto-grants-2011_09