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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37269생성일: 2026년 10월 24일

Water → (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino)-1,3-dioxan-2-yl]pyrrolidine

https://huagongshe.com/ko/reaction/37269

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물p-Toluenesulfonic acidHCID 6101—
반응물(2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 18638815—
반응물2-(4-Nitrobenzyloxycarbonyl)amino-1,3-propanediolHCID 19934522—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino)-1,3-dioxan-2-yl]pyrrolidineHCID 1863881085.7%

반응 단계

A solution of 2-(4-nitrobenzyloxycarbonyl)amino-1,3-propanediol (1.42 g), (2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl) pyrrolidine (1.00 g) and 4-toluene-sulfonic acid (0.30 g) in toluene was refluxed for 2 hours with removing water under azeotropic condition. The reaction mixture was poured into a mixture of water and ethyl acetate. The organic layer was separated, washed with brine, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (80 ml) and eluted with a mixture of acetone and dichloromethane (1:9, V/V) to give (2S, 4S)-4-acetylthio-1- (4-nitrobenzyloxycarbonyl)-2-[5-(4-nitrobenzyloxycarbonylamino) -1,3-dioxan-2-yl]pyrrolidine (1.47 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420122
출처 데이터셋uspto-grants-1995_05
ORD IDord-ae36b222e23a4aec9fa43903c97c4233
출처 메모uspto-grants-1995_05