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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642324Generated: October 26, 2026

N-bromobutanimide → Ethyl 2-bromo-4-(bromomethyl)thiazole-5-carboxylate

https://huagongshe.com/reaction/642324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylateHCID 2824057—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromo-4-(bromomethyl)thiazole-5-carboxylateHCID 6842814059.8%

Reaction Steps

A mixture of 2-Bromo-4-methyl-thiazole-5-carboxylic acid ethyl ester (5.67 g, 22.68 mmol), N-bromosuccinimide (4.44 g, 24.95 mmol) and benzoyl peroxide (275 mg, 1.13 mmol) in carbon tetrachloride (25 mL) was refluxed for 16 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 white solid (4.46 g): MS: (+) m/z 337.80, 329.93, 331.93 (M+1, 79Br/81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-3e84403aeb044e36891e23b048abaf59
Source noteuspto-grants-2010_04