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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299636Generated: October 31, 2026

m-Chloroperbenzoic acid → 1-(N-benzyloxycarbonyl-N-phenylamino)-2,3-epoxypropane

https://huagongshe.com/reaction/2299636

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantbenzyl N-phenyl-N-(prop-2-en-1-yl)carbamateHCID 11448535—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
Product1-(N-benzyloxycarbonyl-N-phenylamino)-2,3-epoxypropaneHCID 1800730837.7%

Reaction Steps

Under nitrogen, to a solution of N-allyl-N-phenyl-benzyloxycarbonylamine (5.5 g) in dichloromethane (50 ml) was added m-chloroperbenzoic acid (3.9 g) at 5° C., and the mixture was stirred at room temperature for 3 days. The resulting mixture was poured into aqueous sodium hydrogensulfite and extracted with ethyl acetate. The organic layer was successively washed with saturated aqueous sodium hydrogencarbonate and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=10:1 to 5:1) to give 1-(N-benzyloxycarbonyl-N-phenylamino)-2,3-epoxypropane (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495546B1
Source datasetuspto-grants-2002_12
ORD IDord-a91b31524c1c492eac97bb3ac9afab58
Source noteuspto-grants-2002_12