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HRID 478049作成日:2026年10月25日

Methyl acetoacetate → Bacampicillin

https://huagongshe.com/reaction/478049

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl acetoacetateHCID 7757—
反応物Ampicillin TrihydrateHCID 23565—
反応物Sodium BicarbonateHCID 516892—
反応物1-Bromoethyl ethyl carbonateHCID 3021550—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物BacampicillinHCID 44139767%

反応条件

温度40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889929
出典データセットuspto-grants-1989_12
ORD IDord-743f45a0d4124d639956a7549ffcf5a7
出典メモuspto-grants-1989_12