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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 478049Erstellt: 24. Oktober 2026

Methyl acetoacetate → Bacampicillin

https://huagongshe.com/de/reaction/478049

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl acetoacetateHCID 7757—
EduktAmpicillin TrihydrateHCID 23565—
EduktSodium BicarbonateHCID 516892—
Edukt1-Bromoethyl ethyl carbonateHCID 3021550—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBacampicillinHCID 44139767%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A mixture of ampicillin trihydrate (15 g), methylaceto acetate (5.65 g), triethylamine (4.05 g) and acetone (7.5 ml) was stirred at 40° C. for 3 hours. Acetone (30 ml) and sodium bicarbonate (12.4 g) were added. 1-Bromoethyl ethyl carbonate (14.6 g) was added dropwise during 1 hour. Stirring was continued at 40° C. for 1 hour. Water (37.5 ml) was added and the reaction was stirred at 20° C. for 1 hour. Ethyl acetate (37.5 ml) was added and the phases separated. The organic phase was washed with 20% sodium chloride solution. Acetone (7.5 ml) was added and a solution of ca. 16% hydrochloric acid was added slowly until a stable pH of 2.2 was obtained. The addition takes 11/2-2 hours. The solution was dried over anhydrous sodium sulfate and filtered. Butyl acetate (45 ml) was added and the solution was evaporated in vacuo to remove most of the solvents (bath temperature 35° C.). More butyl acetate (50 ml) was added and partially distilled. The resulting slurry was cooled for several hours and filtered to give 11.6 g bacampicillin.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04889929
Quelldatensatzuspto-grants-1989_12
ORD IDord-743f45a0d4124d639956a7549ffcf5a7
Quellennotizuspto-grants-1989_12