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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19265Generated: October 26, 2026

Benzoyl Peroxide → (E)-4-bromo-3-(3-chloro-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-(3-chloro-phenoxy)-but-2-enoic acid ethyl esterHCID 66894928—
SolventCarbon TetrachlorideHCID 5943—
Product(E)-4-bromo-3-(3-chloro-phenoxy)-but-2-enoic acid ethyl esterHCID 6689343664.8%

Reaction Steps

To a stirred mixture of (E)-3-(3-chloro-phenoxy)-but-2-enoic acid ethyl ester (3.45 g, 0.014 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (2.79 g, 0.016 mol) and benzoyl peroxide (347 mg, 0.001 mol). Nitrogen gas was bubbled through the mixture for 5 min, and the resulting mixture was heated to reflux for 4 h. The reaction mixture was then placed in the refrigerator overnight. The solids formed were removed by filtration and the filtrate concentrated in vacuo. The crude product obtained was purified using flash column chromatography (silica gel (100-200 mesh), ethyl acetate/hexanes) to afford (E)-4-bromo-3-(3-chloro-phenoxy)-but-2-enoic acid ethyl ester (2.90 g, 63%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-14811994013f4996bd30b1ce42a7a9e9
Source noteuspto-grants-2010_06