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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418197Generated: November 3, 2026

Phosphorus pentachloride → 3-(2-Hydroxyimino-2-phenylacetamido)-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone

https://huagongshe.com/reaction/2418197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
ReactantSodium BicarbonateHCID 516892—
ReactantBistrimethylsilylacetamidHCID 11708267—
ReactantHCID 53748477HCID 53748477—
Reactant3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinoneHCID 53965487—
SolventDichloromethaneHCID 6344—
Product3-(2-Hydroxyimino-2-phenylacetamido)-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinoneHCID 8673704935.7%

Reaction Steps

3-Amino-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (1.3 g.) was added to methylene chloride (30 ml.), and then bis(trimethylsilyl)acetamide (3.05 g.) was added thereto. To the solution, there was dropwise added methylene chloride (30 ml.) solution containing 2-(2,2-dichloroacetoxyimino)-2-phenylacetic acid (1.9 g.) and phosphorus pentachloride (1.7 g.) at -40° to -35° C. in the course of 5 minutes. The mixture was stirred at the same temperature for 15 minutes and additionally stirred at 5° C. for 15 minutes. An aqueous sodium bicarbonate was added to the reaction mixture and the mixture was stirred at ambient temperature for 5 minutes. The methylene chloride layer was separated from the mixture, washed with dilute hydrochloric acid, an aqueous sodium bicarbonate and water in turn, and then dried over magnesium sulfate. The solvent was removed by distillation under reduce pressure to give a residue, which was subjected to column chromatography on silica gel (100 g.). Elution was carried out with chloroform and the fractions containing a desired compound were collected. The solvent was distilled off from the eluate under reduced pressure to give crystals of 3-(2-hydroxyimino-2-phenylacetamido)-1-(2-methoxycarbonyl-1-phenylethyl)-2-azetidinone (0.74 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472300
Source datasetuspto-grants-1984_09
ORD IDord-64f62ea953724f46aeb8eda15ed6c1a2
Source noteuspto-grants-1984_09