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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35733Erstellt: 23. Oktober 2026

Pyridine → Benzeneacetamide

https://huagongshe.com/de/reaction/35733

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktAcetyl bromideHCID 10482—
EduktN,O-bis(trimethylsilyl)acetamideHCID 6913588—
EduktN,N'-bis(trimethylsilyl)sulfamideHCID 13813126—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktBenzeneacetamideHCID 7680—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

0.36 ml (4.5 mmoles) of pyridine were added to a suspension of 0.525 g (1.50 mmoles) of benzylpenicillin sulphoxide in 10 ml of dioxane and the resulting solution was cooled to 0° C. followed by the addition of 0.05 ml (0.5 mmole) of acetyl bromide and the reaction mixture was stirred for 30 minutes at 0° C. 0.49 ml (1.9 mmoles) of N,O-bis(trimethylsilyl)acetamide and 0.38 g (1.6 mmoles) of N,N'-bis-trimethylsilyl sulphamide were added. The mixture was heated to reflux and after 4 hours at reflux, the amount of Δ3 -phenylacetamide desacetoxycephalosporanic acid formed, titrated by a microbiological analysis, was 95%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04767851
Quelldatensatzuspto-grants-1988_08
ORD IDord-acb465f73b04489bbec5774333ac010e
Quellennotizuspto-grants-1988_08