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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903261Generated: October 26, 2026

Benzoyl Peroxide → Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetate

https://huagongshe.com/reaction/1903261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 3,4-dichlorophenylacetateHCID 2737422—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromo-2-(3,4-dichlorophenyl)acetateHCID 12717583—

Reaction Steps

In a three-necked flask fitted with a Nichrome stirrer and a relux condenser is placed 7.0 g. of ethyl 3,4-dichlorophenylacetate, 5.9 g. of N-bromosuccinimide, 0.1 g. of benzoyl peroxide and 150 ml. of carbon tetrachloride. The reaction mixture is heated at reflux for 18 hours, cooled and filtered. The carbon tetrachloride filtrate is concentrated under reduced pressure to give a deep orange liquid. Vacuum distillation at 115°-120° C. (0.5 mm) gives ethyl α-bromo-3,4-dichlorophenylacetate as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435419
Source datasetuspto-grants-1984_03
ORD IDord-c7b43b0287d34961a84ff4f7c72e6a76
Source noteuspto-grants-1984_03