Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903189Generated: October 26, 2026

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

https://huagongshe.com/reaction/903189

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 numberUS04226866
Source datasetuspto-grants-1980_10
ORD IDord-48b00369a8754112b546bede706d65a9
Source noteuspto-grants-1980_10