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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580673Generated: October 26, 2026

Phenacyl bromide → 2-(3,5-Dichlorophenyl)oxirane

https://huagongshe.com/reaction/580673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantStyrene OxideHCID 7276—
ReactantEthyl AcetateHCID 8857—
Reactant3',5'-DichloroacetophenoneHCID 2758058—
SolventChloroformHCID 6212—
Product2-(3,5-Dichlorophenyl)oxiraneHCID 13488795—

Reaction Steps

The phenacyl bromide intermediate for the above-mentioned styrene oxide is prepared by brominating 10 g of 3,5-dichloroacetophenone in 50 ml of CHCl3 /50 ml of EtOAc with 23.6 g of CuBr2. The mixture is heated at reflux for 2.5 hours and cooled to room temperature. After stirring for 16 hours at room temperature, the mixture is cooled in ice for 2 hours and filtered. The filter cake is washed with 50 ml of CHCl3 and the combined filtrates are twice decolorized with activated carbon, filtered, and evaporated to dryness in vacuo to afford the orange oil of the 3,5-dichlorostyrene oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04754047
Source datasetuspto-grants-1988_06
ORD IDord-133da0958dad4eccb03320629cda440b
Source noteuspto-grants-1988_06