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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018053Generated: October 30, 2026

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

https://huagongshe.com/reaction/1018053

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 numberUS06479668B1
Source datasetuspto-grants-2002_11
ORD IDord-c6e943b0bfb94dd0919da16aa1b00df5
Source noteuspto-grants-2002_11