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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34471Generated: October 27, 2026

Benzoyl Peroxide → 3-(1-Bromoethyl)benzophenone

https://huagongshe.com/reaction/34471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant3-EthylbenzophenoneHCID 583730—
SolventCarbon TetrachlorideHCID 5943—
Product3-(1-Bromoethyl)benzophenoneHCID 12802924—

Reaction Steps

Into a 200 ml reactor equipped with a reflux condenser and a stirrer, 60 ml of carbon tetrachloride and 10 g of 3-ethylbenzophenone were introduced. While stirring the resultant mixture at room temperature, 8.6 g of N-bromosuccinimide and 0.14 g of benzoyl peroxide were added thereto, and reflux was performed for 8 hours while stirring the reaction solution. After the reaction solution had been cooled to room temperature, the succinimide was filtered out, and carbon tetrachloride was distilled off from a filtrate under a reduced pressure. The spectrum data of the obtained product were in accord with those of 3-(1-bromoethylbenzophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761508
Source datasetuspto-grants-1988_08
ORD IDord-808cbc7c67484e6e8b9a7ce6224107ab
Source noteuspto-grants-1988_08