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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418190Generated: November 3, 2026

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

https://huagongshe.com/reaction/2418190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant3-[(Phenylacetyl)amino]-2-azetidinoneHCID 13212048—
ReactantBenzyl 2-bromo-2-phenylacetateHCID 20445638—
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 numberUS04472300
Source datasetuspto-grants-1984_09
ORD IDord-e9f59aa90891487caecfeabc6e099975
Source noteuspto-grants-1984_09