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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706526Generated: October 31, 2026

Methanol → 3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone

https://huagongshe.com/reaction/1706526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChloroformHCID 6212—
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
ReactantHCID 23463638HCID 23463638—
SolventEthyl AcetateHCID 8857—
Product3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinoneHCID 5396548782.6%

Reaction Steps

3-Phthalimido-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (1.90 g.) and N,N-dimethyl-1,3-propanediamine (1.14 g.) were added to a mixture of methanol (20 ml.) and chloroform (5 ml.), whereafter the mixture was stirred at ambient temperature for 17 hours. The reaction mixture was evaporated to dryness under reduced pressure to give a residue, which was dissolved in ethyl acetate (20 ml.). The solution was extracted with three portions of an aqueous solution consisting of 1 N hydrochloric acid (5.3 ml.) and water (11.3 ml.), and then the combined extract was washed with ethyl acetate. The aqueous solution was adjusted to pH 8 with sodium bicarbonate under ice-cooling and then extracted with three 10 ml. portions of chloroform. The extracts were washed with water and then dried over magnesium sulfate. The solvent was removed by distillation from the solution under reduced pressure to give oily 3-amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (1.030 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207234
Source datasetuspto-grants-1980_06
ORD IDord-67c3f9330db54dec966e098c979dc729
Source noteuspto-grants-1980_06