Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719125Generated: November 1, 2026

Benzoyl Peroxide → 2-bromo-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime

https://huagongshe.com/reaction/719125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oximeHCID 73852544—
SolventCarbon TetrachlorideHCID 5943—
Product2-bromo-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oximeHCID 7385254580%

Reaction Steps

To a solution of 1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime (1.120 g, 4.214 mmol) in carbon tetrachloride were added N-bromosuccinimide (812 mg, 4.425 mmol) and benzoyl peroxide (102 mg, 0.4 mmol). The resulting mixture was heated at reflux for 12 h. Upon cooling to room temperature, the solids were filtered and washed with diethyl ether. The filtrate was washed with aqueous solution of sodium bicarbonate, sodium thiosulfate and brine. It was then dried with anhydrous sodium sulfate and concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32–63 μm, 60 Å silica gel) eluting with 1–2% ethyl acetate in hexanes yielded 2-bromo-1-(4-chloro-phenyl)-3-cyclopentyl-propan-1-one O-methyl-oxime (1.16 g, 80%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132421B2
Source datasetuspto-grants-2006_11
ORD IDord-d099b848a5c6466c850a0ea8c2f83cdf
Source noteuspto-grants-2006_11