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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568836Generated: October 25, 2026

Benzoyl Peroxide → Ethyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetate

https://huagongshe.com/reaction/568836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetateHCID 53737196—
SolventBenzeneHCID 241—
ProductEthyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetateHCID 5389498994.3%

Reaction Steps

A small amount of benzoyl peroxide was added to a suspension of ethyl 2(2-formamidothiazol-4-yl)-2-methoxyiminoacetate (syn isomer, 7.55 g.) and N-bromosuccinimide (5.75 g.) in dry benzene (150 ml.) and refluxed under heating for an hour. After cooling, the reaction mixture was washed with water three times, dried over magnesium sulfate, treated with activated charcoal and then evaporated in vacuo. The residue was pulverized with n-hexane, and the precipitates were collected by filtration, washed with n-hexane and water successively and dried to give ethyl 2-(2-formamido-5-bromothiazol-4-yl)-2-methoxyiminoacetate (syn isomer, 9.3 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04729991
Source datasetuspto-grants-1988_03
ORD IDord-92a1c6d0c83a42498cc3554908449f1e
Source noteuspto-grants-1988_03