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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281284Generated: November 1, 2026

m-Chloroperbenzoic acid → 4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one

https://huagongshe.com/reaction/2281284

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-methyl-5-vinylisobenzofuran-1(3H)-oneHCID 66643922—
SolventDichloromethaneHCID 6344—
Product4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-oneHCID 55270555—

Reaction Steps

5-ethenyl-4-methyl-2-benzofuran-1(3H)-one (1.5 g, 8.4 mmol) was added to DCM (25 mL) at 0° C. then meta-chloroperbenzoic acid (2.9 g, 17 mmol) was added and the mixture was stirred at RT overnight. The reaction mixture was washed once each with saturated aqueous Na2S2O3, saturated sodium bicarbonate, and brine. The organic layer was dried over Na2SO4, filtered, and evaporated to dryness. The crude material was purified by MPLC chromatography (eluting with 0-80% EtOAc/hexane solvent system) to yield 4-methyl-5-oxiran-2-yl-2-benzofuran-1(3H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139585B2
Source datasetuspto-grants-2015_09
ORD IDord-28027ab7f72c4b93abe20576f63771b4
Source noteuspto-grants-2015_09