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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1032353Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1032353

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-BromoacetamideHCID 4353—
EduktSodium ChlorideHCID 5234—
EduktSodium ThiosulfateHCID 24477—
Edukt1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-(methylthio)-2-azetidinoneHCID 86737252—
LösungsmittelMethanolHCID 887—
Produkt1-(Benzyloxycarbonyldiethylphosphono)methyl-3-azido-4-methylsulfonyl-2-azetidinoneHCID 86737251—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04957912
Quelldatensatzuspto-grants-1990_09
ORD IDord-428b98e828e94a269771bea05d804bbe
Quellennotizuspto-grants-1990_09