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HRID 867652作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Trimethylsilyl chlorosulphateHCID 78059—
反応物(trans)-3-t-Butoxycarbonylamino-4-ethyl-2-azetidinoneHCID 70415750—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(trans)-3-t-Butoxycarbonylamino-4-ethyl-2-oxo-1-azetidinesulfonic acid, tetrabutylammonium saltHCID 131714274—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04775670
出典データセットuspto-grants-1988_10
ORD IDord-fa0f256c32194f73a8606b838678c3b8
出典メモuspto-grants-1988_10