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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961696Generated: October 31, 2026

Benzoyl Peroxide → 4-(Bromomethyl)-2-chloro-1-(trifluoromethyl)benzene

https://huagongshe.com/reaction/1961696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-4-methylbenzotrifluorideHCID 2736619—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-2-chloro-1-(trifluoromethyl)benzeneHCID 2351276580.4%

Reaction Steps

A mixture of 2-chloro-4-methyl-1-trifluoromethylbenzene 26 (0.20 g, 1 mmol), N-bromosuccinimide (0.17 g, 1 mmol) and benzoyl peroxide (7.4 mg, 0.03 mmol) in carbon tetrachloride (2 mL) was heated to reflux for 2 hours. Another portion of benzoyl peroxide (20 mg, 0.08 mmol) was added. The mixture was heated to reflux for another 0.5 hours. The reaction mixture was further stirred at room temperature for 16 hours. The solid was removed by filtration. The solvent was removed under reduced pressure. The crude product was purified by flash chromatography on silica, using petroleum ether as eluent, to give 0.22 g (80%) of Compound 27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415357B2
Source datasetuspto-grants-2013_04
ORD IDord-53866a1148144b11bd6d8c80e4783603
Source noteuspto-grants-2013_04