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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269222Generated: October 31, 2026

Benzoyl Peroxide → (3-bromoprop-1-en-2-yl)benzene

https://huagongshe.com/reaction/2269222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantAlpha-MethylstyreneHCID 7407—
ReactantN-bromobutanimideHCID 67184—
SolventBenzeneHCID 241—
Product(3-bromoprop-1-en-2-yl)benzeneHCID 23499851.5%

Reaction Steps

Benzene (120 ml), was mixed with 9.00 g (76.2 mmol), of α-methylstyrene, 14.2 g (80.0 mmol), of N-bromosuccinimide, and 300 mg of benzoyl peroxide and the mixture was refluxed for 24 hours. After the solvent was distilled off under reduced pressure, carbon tetrachloride was added and the resulting crystals were filtered. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (n-hexane 100%), to obtain the target compound. The yield, % yield and NMR spectrum were as follows. Yield: 7.72 g, % yield: 51.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329399B1
Source datasetuspto-grants-2001_12
ORD IDord-d96042b0e100448e8e8f383712c7d801
Source noteuspto-grants-2001_12