Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366876Generated: October 30, 2026

Water → 3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexane

https://huagongshe.com/reaction/366876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-Chlorobenzenesulfonic acidHCID 7400—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant1-Benzyl-2,5-dihydropyrroleHCID 561506—
SolventAcetoneHCID 180—
Product3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexaneHCID 981537095.9%

Reaction Steps

To a solution of 15.9 g (0.1 mol) of 1-benzyl-3-pyrroline, 46.2 g (0.24 mol) of p-chlorobenzenesulfonic acid (produced by Tokyo Chemical Industry Co., Ltd.), 15.0 g of water, and 60.0 g of acetone in a round flask reactor, 31.1 g (0.13 mol) of 70% m-CPBA (m-chloroperbenzoic acid produced by Tokyo Chemical Industry Co., Ltd.) was added with stirring and allowed to react for 10 hours at room temperature without irradiation by lamps. After completion, acetone was evaporated under reduced pressure, neutralized by NaOH (aq), and extracted with toluene and water. After the solvent was evaporated under reduced pressure, 16.8 g of 1-benzyl-3,4-epoxypyrrolidine (yield 95.9%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130338
Source datasetuspto-grants-2000_10
ORD IDord-b4ce81bd097a467e87fb3c4ad0e3d6bc
Source noteuspto-grants-2000_10