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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224315Generated: October 31, 2026

Benzoyl Peroxide → 2-(4-(Bromomethyl)phenyl)benzo[d]thiazole

https://huagongshe.com/reaction/224315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(4-Methylphenyl)-1,3-benzothiazoleHCID 919385—
SolventCarbon TetrachlorideHCID 5943—
Product2-(4-(Bromomethyl)phenyl)benzo[d]thiazoleHCID 1327672967.4%

Reaction Steps

To a solution of 45 g (0.2 mol) of 4-(benzothiazol-2-yl) toluene in 1000 ml of dry carbon tetrachloride were added 35.6 g (0.2 mol) of N-bromosuccinimide and a catalytic amount of benzoyl peroxide. The mixture was refluxed for 12 hours, and then allowed to cool down to room temperature. The precipitated succinimide was filtered off and the filtrate evaporated to dryness in vacuo, whereupon 55 g of crude crystals were obtained. Recrystallization from 1500 ml of cyclohexane gave 41 g of purified 4-(benzothiazol-2-yl) bromomethylbenzene as colorless flakes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232010
Source datasetuspto-grants-1980_11
ORD IDord-d62e145b728e4e42b4ad7a36cfd34c4b
Source noteuspto-grants-1980_11