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HRID 867652생성일: 2026년 10월 24일

Pyridine → (trans)-3-t-Butoxycarbonylamino-4-ethyl-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium salt

https://huagongshe.com/ko/reaction/867652

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Trimethylsilyl chlorosulphateHCID 78059—
반응물(trans)-3-t-Butoxycarbonylamino-4-ethyl-2-azetidinoneHCID 70415750—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(trans)-3-t-Butoxycarbonylamino-4-ethyl-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 131714274—

반응 단계

To 2 ml of absolute pyridine in 20 ml of dry dichloromethane is added trimethylsilyloxysulfonyl chloride (3.7 ml) in 5 ml of dry dichloromethane. The addition is accomplished at -30° C., under nitrogen, over a 10 minute period. After stirring at ambient temperature for 30 minutes, the flask is evacuated to yield a pyridine-sulfur trioxide complex. (trans)-3-t-Butoxycarbonylamino-4-ethyl-2-azetidinone (2.67 g) and 20 ml of dry pyridine are added to the flask which is then placed in an oil bath preheated to 90° C. After 15 minutes a clear solution is obtained and poured into 200 ml of a 1M solution of dibasic potassium phosphate. After the addition of 27 g of dibasic potassium phosphate and 100 ml of water a clear solution is obtained. The solution is extracted with two 60 ml portions of ethyl acetate. Tetrabutylammonium hydrogensulfate is added to the aqueous layer, and the aqueous solution is extracted with three 100 ml portions of dichloromethane and the combined organic layers are dried over MgSO4. Concentration in vacuo yields 6.9 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04775670
출처 데이터셋uspto-grants-1988_10
ORD IDord-fa0f256c32194f73a8606b838678c3b8
출처 메모uspto-grants-1988_10