Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19246Generated: October 29, 2026

Benzoyl Peroxide → HCID 66894842, compound

https://huagongshe.com/reaction/19246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant(E)-3-(2-benzyloxy-phenoxy)-but-2-enoic acid ethyl esterHCID 66894914—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 66894842HCID 6689484265.3%

Reaction Steps

To a stirred mixture of (E)-3-(2-benzyloxy-phenoxy)-but-2-enoic acid ethyl ester (5.70 g, 0.018 mol) in carbon tetrachloride (35 mL) under a nitrogen atmosphere was added N-bromosuccinimide (4.90 g, 0.028 mol) and benzoyl peroxide (440 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)-3-(2-benzyloxy-phenoxy)-4-bromo-but-2-enoic acid ethyl ester (4.60 g, 64%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-bb427e48e6364ecbb3db55538a859d39
Source noteuspto-grants-2010_06