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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175759Generated: October 29, 2026

m-Chloroperbenzoic acid → 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one

https://huagongshe.com/reaction/2175759

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-ethenyl-2-benzofuran-1(3H)-oneHCID 21106313—
SolventDichloromethaneHCID 6344—
Product5-(oxiran-2-yl)-2-benzofuran-1(3H)-oneHCID 59568715—

Reaction Steps

5-Ethenyl-2-benzofuran-1(3H)-one (28.4 g, 177 mmol) was dissolved in DCM (400 mL) then mCPBA (47.7 g, 213 mmol) was added. The mixture was stirred at room temperature overnight. Some starting olefin remained. Another 25 g of mCPBA was added and the mixture was stirred overnight. The mixture was poured into ice cold Na2SO3 solution (saturated). The layers were separated and the organic layer was washed with 5% NaOH solution, brine, then was dried (MgSO4). The crude product was purified by MPLC (330 g column, eluting with 40% EtOAc/hexane, 2 L, then with 45% EtOAc/hexane, 2 L, to afford 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one. LC-MS: M+1=177.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-8dbc2dac70874230a568adc472040142
Source noteuspto-grants-2015_06