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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508117Generated: October 29, 2026

Benzoyl Peroxide → HCID 117690398, compound

https://huagongshe.com/reaction/508117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 117690248HCID 117690248—
SolventEthyl AcetateHCID 8857—
ProductHCID 117690398HCID 11769039885%

Reaction Steps

A stirred solution of 1-[1-(2-chlorophenyl)prop-1-en-2-yl]-2,4-difluorobenzene (680 mg, 2.56 mmol), N-bromosuccinimide (823 mg, 4.62 mmol) and benzoyl peroxide (30 mg) in AcOEt (15 ml) was heated under reflux for 3 h. After cooling to room temperature, the reaction mixture was diluted with AcOEt and washed with water, and the combined organic phases were dried and concentrated to dryness under reduced pressure. Purification by chromatography on silica gel gave 1-[3-bromo-1-(2-chlorophenyl)prop-1-en-2-yl]-2,4-difluorobenzene as a 52/48 mixture of diastereoisomers [colourless oil, 792 mg, yield 85%; GC/MS: m/z=344 (M+); HPLC/MS: log P(HCOOH)=4.80 (major diastereoisomer), 5.25 (minor diastereoisomer)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09095136B2
Source datasetuspto-grants-2015_08
ORD IDord-58626a37a0714ac98fdb54e9d9308a75
Source noteuspto-grants-2015_08