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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706512Generated: October 29, 2026

Ethyl Acetate → 1-(alpha-Benzyloxycarbonylbenzyl)-3-(2-phenyl)acetamido-2-azetidinone

https://huagongshe.com/reaction/1706512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3-[(Phenylacetyl)amino]-2-azetidinoneHCID 13212048—
ReactantBenzyl 2-bromo-2-phenylacetateHCID 20445638—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
Product1-(alpha-Benzyloxycarbonylbenzyl)-3-(2-phenyl)acetamido-2-azetidinoneHCID 15592316—

Reaction Steps

3-(2-Phenylacetamido)-2-azetidinone (816 mg.) and benzyl 2-bromo-2-phenylacetate (1.22 g.) were dissolved in N,N-dimethylformamide (20 ml.), and to the solution was added sodium hydride (50% oily) (210 mg.) in nitrogen atmosphere under ice-cooling while stirring, and then the reaction mixture was stirred for an hour at the same temperature. Ethyl acetate (150 ml.) was added to the reaction mixture, and the solution was washed with water, a sodium bicarbonate-saturated-aqueous solution and water respectively, and then dried over anhydrous magnesium sulfate. The solution was evaporated to dryness under reduced pressure to give the yellow oily material (1.7 g.). The material was subjected to column chromatography using silica.gel (developer: chloroform) to give two isomers of 1-(α-benzyloxycarbonylbenzyl)-3-(2-phenyl)acetamido-2-azetidinone. Yield of the isomer A is 26 mg. and it of the isomer B is 65 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207234
Source datasetuspto-grants-1980_06
ORD IDord-40da6923c7ba467aa3c9fc528154593e
Source noteuspto-grants-1980_06