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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297928Generated: October 30, 2026

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

https://huagongshe.com/reaction/2297928

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-1-phenyl-3,4-epoxy-butane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492400B1
Source datasetuspto-grants-2002_12
ORD IDord-fc917665a446457593f433f214851dea
Source noteuspto-grants-2002_12