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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1576297Erstellt: 26. Oktober 2026

Amoxicillin Trihydrate → 6-Aminopenicillanic acid

https://huagongshe.com/reaction/1576297

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmoxicillin TrihydrateHCID 62883—
EduktAmoxicillin hydrochlorideHCID 67247297—
Produkt6-Aminopenicillanic acidHCID 11082—
ProduktAmoxicillin TrihydrateHCID 62883—

Reaktionsschritte

A procedure for the preparation of amoxicillin trihydrate via anhydrous acylation and isolation via the amoxicillin hydrochloride intermediate is set forth above. 2. Lab experiments gave 77 to 82% activity yields to amoxicillin trihydrate from 6-APA. A normal isolation leaves 6 to 9% activity assayed as amoxicillin in the salt mother liquor; 2 to 3% amoxicillin in the LA-1 mother liquor and approximately 3% unreacted 6-APA.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03980637
Quelldatensatzuspto-grants-1976_09
ORD IDord-ba78d49b542d41bdbf7886ceaa1e68c7
Quellennotizuspto-grants-1976_09