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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577244Generated: October 28, 2026

Benzoyl Peroxide → HCID 59589488, compound

https://huagongshe.com/reaction/577244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactantα,5-Dimethyl-4-thiazolemethanolHCID 21313043—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 59589488HCID 5958948840%

Reaction Steps

To a solution of 1-(5-methyl-1,3-thiazol-4-yl)ethan-1-ol (1.0 g, 7.0 mmol) in anhydrous carbon tetrachloride (50 mL) was added recrystallized 1-bromopyrrolidine-2,5-dione (1.4 g, 7.7 mmol) and benzoyl benzenecarboperoxoate (170 mg, 0.7 mmol). The mixture was stirred at reflux for 5 hours. After cooling to room temperature, the solid material was removed by filtration. The filtrate was recovered and evaporated. The residue was dried in vacuo, affording 1-[5-(bromomethyl)-1,3-thiazol-4-yl]ethan-1-one (615 mg, 40%). The product was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-e5e9ec420d9a4511a82ae4cd89716519
Source noteuspto-grants-2015_05