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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19231Generated: October 25, 2026

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

https://huagongshe.com/reaction/19231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl esterHCID 66895456—
SolventCarbon TetrachlorideHCID 5943—
Product(E)-4-bromo-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl esterHCID 6689534840%

Reaction Steps

To a stirred mixture of (E)-3-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl ester (8.01 g, 0.033 mol) in carbon tetrachloride (30 mL) under a nitrogen atmosphere was added N-bromosuccinimide (8.91 g, 0.050 mol) and benzoyl peroxide (810 mg, 0.003 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-(2,3-difluoro-phenoxy)-but-2-enoic acid ethyl ester (4.20 g, 40%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-57afde570ecf42ffa3ed381edaac9547
Source noteuspto-grants-2010_06