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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642294Generated: October 25, 2026

N-bromobutanimide → 4-Bromomethyl-2-(4-methoxy-phenyl)-thiazole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-(4-methoxyphenyl)-4-methyl-1,3-thiazole-5-carboxylateHCID 7540952—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromomethyl-2-(4-methoxy-phenyl)-thiazole-5-carboxylic acid ethyl esterHCID 6842741894.3%

Reaction Steps

A mixture of 2-(4-Methoxy-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester (1.41 g, 5.09 mmol), N-bromosuccinimide (951 mg, 5.34 mmol) and benzoyl peroxide (62 mg, 0.25 mmol) in carbon tetrachloride (20 mL) was refluxed for 15 h before it was cooled to room temperature and partitioned between dichloromethane and water, the organic layer was washed with saturated aqueous sodium bicarbonate solution, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a yellow solid (1.71 g): MS: (+) m/z 355.96, 357.96 (M+1, 79Br/81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-084115644596457d9a8a75ade597e29d
Source noteuspto-grants-2010_04