돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2073253생성일: 2026년 10월 25일

Potassium sodium tartarate → (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine

https://huagongshe.com/reaction/2073253

반응식

참여 물질

역할이름HCID투입량
반응물Potassium sodium tartarateHCID 9855836—
반응물(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidineHCID 14772685—
반응물DiisobutylaluminumhydrideHCID 21225700—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물(2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidineHCID 1567037765.9%

반응 조건

온도-78 °C

반응 단계

To a solution of (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-methoxycarbonylpyrrolidine (9.01 g) in toluene (70 ml) was added dropwise 1.5 molar solution of diisobutylaluminum hydride (61.2 m mol) in tetrahydrofuran (40.8 ml) at -78° C. After the mixture was stirred at -78° C. for 1.5 hours, saturated aqueous potassium sodium tartrate was added to the reaction mixture and the mixture was filtered through Celite. The solid was washed with ethyl acetate and the combined organic solution was washed with brine and dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was chromatographed on a silica gel column with a mixture of ethyl acetate and n-hexane (1:2-2:1) as an eluent to give (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine (5.51 g) as pale yellow crystal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04916152
출처 데이터셋uspto-grants-1990_04
ORD IDord-1615f33cf72341f1b70f465910f68ced
출처 메모uspto-grants-1990_04