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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493501Generated: October 30, 2026

Benzoyl Peroxide → 2-(Bromomethyl)-7-chloroquinoline

https://huagongshe.com/reaction/1493501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Chloro-2-methylquinolineHCID 138395—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-7-chloroquinolineHCID 1024416048.9%

Reaction Steps

A stirred suspension of 7-chloroquinaldine (18.0 g, 0.10 mol), N-bromosuccinimide (18.0 g, 0.10 mol), and benzoyl peroxide (1.0 g, 0.004 mol) in CCl4 (400 mL) is illuminated with a 300 W reflector bulb for 6 hours. The reaction mixture is cooled and filtered through a plug of silica using hexane:ethyl acetate (7:3). The yellow filtrate is concentrated to give a crude mixture of unreacted starting material together with the monobromo and less polar dibromo products. The crude material is purified by flash chromatography (preabsorbed on silica Merck 60 with methylene chloride and then eluted with hexane:ethyl acetate 95:5), to yield fairly pure title product as an off-white solid. (17.31 g, 48.9% yield based on recovered starting material, m.p. 111°-112° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021576
Source datasetuspto-grants-1991_06
ORD IDord-27cacb868b314d18b5ccba2305c65940
Source noteuspto-grants-1991_06