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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474337Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 59568716, compound

https://huagongshe.com/reaction/1474337

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 66643889HCID 66643889—
SolventDichloromethaneHCID 6344—
ProductHCID 59568716HCID 59568716—

Reaction Steps

A solution of 7-fluoro-4-methyl-5-vinyl-3H-isobenzofuran-1-one (420 mg, 1.71 mmol) in 10 mL of DCM was slowly added mCPBA (741 mg, 85% purity, 3.43 mmol) in 10 mL of DCM at 0° C. After warming to room temperature, the mixture was stirred overnight. The mixture was washed with aqueous Na2SO3 until KI paper didn't change color. The organic layers was washed with brine and then concentrated. The residue was purified by column chromatography to give product 7-fluoro-4-methyl-5-oxiranyl-3H-isobenzofuran-1-one. The enantiomers of the product were resolved via SFC (Column Chiralpak AD-H 250*4.6 mm I.D., 5 μm; Mobile phase: methanol (0.05% DEA) in CO2 from 5% to 40%; Flow rate: 2.35 mL/min; Wavelength: 220 nm). MS m/z 209 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-2efc60ce1c89433da3c4017f284556af
Source noteuspto-grants-2015_04