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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070755Generated: October 25, 2026

m-Chloroperbenzoic acid → 2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dione

https://huagongshe.com/reaction/1070755

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantN-(3-Buten-1-yl)phthalimideHCID 339432—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product2-[2-(oxiran-2-yl)ethyl]-2,3-dihydro-1H-isoindole-1,3-dioneHCID 339433—

Reaction Conditions

Temperature0 °C

Reaction Steps

70 g (350 mmol) 2-(but-3-enyl)-isoindolin-1,3-dione are dissolved in dichloromethane. The solution is cooled to ca. 0° C. and a suspension of 120.8 g (350 mmol) 50% 3-chloro-peroxy-benzoic acid in dichloromethane is added under cooling. The mixture is left standing without further cooling at room temperature for two days. After addition of 250 ml saturated NaHCO3 solution the organic phase is separated and washed three times each with 200 ml saturated NaHCO3 solution and once with water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum: yield 80 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903118B1
Source datasetuspto-grants-2005_06
ORD IDord-b214c1b3a19d4f26a1c32cb490e950fe
Source noteuspto-grants-2005_06