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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19066Generated: October 27, 2026

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

https://huagongshe.com/reaction/19066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(4-Methoxy-phenoxy)-but-2-enoic acid ethyl esterHCID 66894795—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl esterHCID 6689543578.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester (0.98 g, 4.17 mmol) in carbon tetrachloride (23.2 mL) was treated with N-bromosuccinimide (0.81 g, 4.59 mmol) and benzoyl peroxide (81 mg, 0.33 mmol). The reaction was then heated to reflux for 5 h. At this time, the reaction was cooled to 25° C. and then was placed in the freezer over the weekend. At this time, the reaction was removed from the freezer and allowed to thaw. The resulting precipitate was removed by filtration and was rinsed with carbon tetrachloride (5 mL). The filtrate was concentrated in vacuo. Purification by Analogix flash chromatography (40 g, 1-4% ethyl acetate/hexanes) afforded impure 4-bromo-3-(4-methoxy-phenoxy)-but-2-enoic acid ethyl ester (1.03 g, 78%) as a pale, yellow oil. The material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-007e44bde25340908035797ba6283bda
Source noteuspto-grants-2010_06