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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455205Generated: October 31, 2026

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

https://huagongshe.com/reaction/1455205

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 irridiated 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 numberUS07482366B2
Source datasetuspto-grants-2009_01
ORD IDord-e87d743d2df045f18c8ee505e758e042
Source noteuspto-grants-2009_01