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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19270Generated: October 26, 2026

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

https://huagongshe.com/reaction/19270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-(3-methoxy-phenoxy)-but-2-enoic acid ethyl esterHCID 66894839—
SolventCarbon TetrachlorideHCID 5943—
Product(E)-4-bromo-3-(3-methoxy-phenoxy)-but-2-enoic acid ethyl esterHCID 6689449855.2%

Reaction Steps

To a stirred mixture of (E)-3-(3-methoxy-phenoxy)-but-2-enoic acid ethyl ester (5.50 g, 0.023 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (6.22 g, 0.035 mol) and benzoyl peroxide (563 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-(3-methoxy-phenoxy)-but-2-enoic acid ethyl ester (4.00 g, 55%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-d16a5bf1c8b44ea39a3af05683e128de
Source noteuspto-grants-2010_06