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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165064Generated: October 31, 2026

Benzoyl Peroxide → 5-Bromo-2-(bromomethyl)-1,3-benzothiazole

https://huagongshe.com/reaction/2165064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Bromo-2-methylbenzothiazoleHCID 3017457—
SolventCarbon TetrachlorideHCID 5943—
Product5-Bromo-2-(bromomethyl)-1,3-benzothiazoleHCID 14458642—

Reaction Steps

A mixture of 2-methyl-5-bromobenzothiazole (32.0 g), N-bromosuccinimide (25.1 g), carbon tetrachloride (700 ml) and a catalytic amount of benzoyl peroxide (0.2 g) was refluxed under irradiation by an UV lamp for 14 hours. The reaction mixture was cooled to room temperature, filtered to remove the precipitated succinimide and the filtrate was evaporated to dryness. The resulting solid was chromatographed over silica gel to obtain the product (7.8 g; m.p. 107° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939140
Source datasetuspto-grants-1990_07
ORD IDord-68dea79663254e25a8d94dd5074b23f0
Source noteuspto-grants-1990_07