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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275876Generated: October 30, 2026

Benzoyl Peroxide → Ethyl 2-(bromomethyl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1275876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-methyl-1,3-thiazole-4-carboxylateHCID 293353—
SolventChloroformHCID 6212—
ProductEthyl 2-(bromomethyl)-1,3-thiazole-4-carboxylateHCID 11043146—

Reaction Steps

2-Methyl-4-thiazolecarboxylic acid ethyl ester (1 g) (Liebigs Ann. Chem. 1981, 623), N-bromosuccinimide (1.04 g) and a catalytic amount of benzoyl peroxide in chloroform (25 ml) was heated at reflux for 20 hours. After cooling, the reaction mixture was washed with saturated aqueous sodium bicarbonate, dried (MgSO4) and evaporated under reduced pressure. Purification was by chromatography eluting with 40% ethyl acetate in isohexane to give the product as an oil. Yield 0.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162808
Source datasetuspto-grants-2000_12
ORD IDord-4362875e2d8d4b4fbdb89a614c12f7c4
Source noteuspto-grants-2000_12