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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032353Generated: October 26, 2026

N-Bromoacetamide → 1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinone

https://huagongshe.com/reaction/1032353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BromoacetamideHCID 4353—
ReactantSodium ChlorideHCID 5234—
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(methylthio)-2-azetidinoneHCID 86737252—
SolventMethanolHCID 887—
Product1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinoneHCID 86737251—

Reaction Steps

1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(methylthio)-2-azetidinone (0.44 g.) is dissolved in methanol (20 ml.) and treated with N-bromoacetamide (0.52 g.) for two hours. Sodium thiosulfate (10 ml.; 0.1N) is then added and the mixture is allowed to stir for five minutes. At the end of this time, the reaction mixture shows no positive reaction to starch iodide paper. The reaction mixture is saturated with sodium chloride and extracted with methylene chloride. The methylene chloride extract is dried and evaporated. The residue is chromatographed to afford 1-(benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957912
Source datasetuspto-grants-1990_09
ORD IDord-428b98e828e94a269771bea05d804bbe
Source noteuspto-grants-1990_09