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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182495Generated: November 1, 2026

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

https://huagongshe.com/reaction/2182495

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 numberUS06897234B2
Source datasetuspto-grants-2005_05
ORD IDord-37de15a4d8ca4b1e846b74fb437f039f
Source noteuspto-grants-2005_05