Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515106Generated: October 27, 2026

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

https://huagongshe.com/reaction/515106

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 room temperature 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 numberUS09108947B2
Source datasetuspto-grants-2015_08
ORD IDord-6d2fc5545159459da5eddd34c1e521c4
Source noteuspto-grants-2015_08