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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171661Generated: November 3, 2026

Benzoyl Peroxide → HCID 23139035, compound

https://huagongshe.com/reaction/1171661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant853804-82-7HCID 23138773—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 23139035HCID 2313903584.5%

Reaction Steps

To a solution of 2-(2,4-difluorophenyl)-1-cyclopropylethanone (329 mg) in carbon tetrachloride (10 ml) was added N-bromosuccinimide (360 mg) and 75% benzoyl peroxide with stirring at room temperature, and the resulting mixture was refluxed for 3.5 hours. After the reaction mixture was filtrated, 1N aqueous sodium hydroxide solution was added to the filtrate. The resulting mixture was extracted with ethyl acetate, and the extract was washed with saturated sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, and the solvent was removed in vacuo to afford the title compound (390 mg, yield: 84%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-194ac7653146420b868ad286e5a3f138
Source noteuspto-grants-2010_11