돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 439405생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/439405

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 번호US05514701
출처 데이터셋uspto-grants-1996_05
ORD IDord-3c165684c0cd4f868b0b80497746ab99
출처 메모uspto-grants-1996_05