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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 478049생성일: 2026년 10월 24일

Methyl acetoacetate → Bacampicillin

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

반응식

참여 물질

역할이름HCID투입량
반응물Methyl acetoacetateHCID 7757—
반응물Ampicillin TrihydrateHCID 23565—
반응물Sodium BicarbonateHCID 516892—
반응물1-Bromoethyl ethyl carbonateHCID 3021550—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물BacampicillinHCID 44139767%

반응 조건

온도40 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04889929
출처 데이터셋uspto-grants-1989_12
ORD IDord-743f45a0d4124d639956a7549ffcf5a7
출처 메모uspto-grants-1989_12