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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66285Generated: October 25, 2026

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

https://huagongshe.com/reaction/66285

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 reflux 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 numberUS04131611
Source datasetuspto-grants-1978_12
ORD IDord-8bb4d254d7f440ec8351d60f1eca7e2b
Source noteuspto-grants-1978_12