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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278707Generated: November 1, 2026

m-Chloroperbenzoic acid → 2-Benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butane

https://huagongshe.com/reaction/1278707

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Benzyloxycarbonylamino-1-phenyl-3-buteneHCID 13606586—
SolventEthyl AcetateHCID 8857—
Product2-Benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butaneHCID 14887243—

Reaction Steps

To a stirred solution of 2-benzyloxycarbonylamino-1-phenyl-3-butene (1.43 g, 5.08 mmoles) in 20 mL of CH2C12 was added 3-chloroperoxybenzoic acid (2.19 g, 60%, 7.62 mmoles) in several portions, and the mixture was stirred at room temperature for 30 hrs. After addition of EtOAc (60 mL), the mixture was washed with saturated NaHCO3 and brine, and the organic layer was dried over Na2SO4. Evaporation of the solvent afforded an oily residue. The crude product was purified by column chromatography on silica gel with elution by 2:8 EtOAc-hexane to give pure 2-benzyloxycarbonylamino-l-phenyl-3,4-epoxy-butane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444686B1
Source datasetuspto-grants-2002_09
ORD IDord-101e66687bd244afab3b481e5ed43341
Source noteuspto-grants-2002_09