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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071367Generated: November 2, 2026

Ethyl Acetate → 2-Benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butane

https://huagongshe.com/reaction/1071367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Benzyloxycarbonylamino-1-phenyl-3-buteneHCID 13606586—
SolventDichloromethaneHCID 6344—
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 CH2Cl2 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. Part C: Preparation of 2-benzyloxycarbonylamino-4-[4-(4-fluorophenyl)methyl-1-piperidinyl]-1-phenyl-butan-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906066B2
Source datasetuspto-grants-2005_06
ORD IDord-bf857adc590c4dba9abf87f6784952f6
Source noteuspto-grants-2005_06