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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19295Generated: October 29, 2026

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

https://huagongshe.com/reaction/19295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-phenoxy-but-2-enoic acid ethyl esterHCID 5356939—
SolventCarbon TetrachlorideHCID 5943—
Product(E)-4-bromo-3-phenoxy-but-2-enoic acid ethyl esterHCID 6689514574.5%

Reaction Steps

To a stirred mixture of (E)-3-phenoxy-but-2-enoic acid ethyl ester (5.00 g, 0.024 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (6.50 g, 0.037 mol) and benzoyl peroxide (580 mg, 0.002 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-phenoxy-but-2-enoic acid ethyl ester (5.10 g, 74%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-137bc97d158748f98a9f507b3ca5d1fc
Source noteuspto-grants-2010_06