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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19236Generated: October 27, 2026

Benzoyl Peroxide → HCID 66894821, compound

https://huagongshe.com/reaction/19236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl esterHCID 66894688—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 66894821HCID 6689482143%

Reaction Steps

To a stirred mixture of (E)-3-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl ester (3.25 g, 0.012 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (3.20 g, 0.018 mol) and benzoyl peroxide (290 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-(2,5-dichloro-phenoxy)-but-2-enoic acid ethyl ester (1.80 g, 43%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-4403dbd3f77441c0bd39621097806c60
Source noteuspto-grants-2010_06