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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37267생성일: 2026년 10월 24일

Thioacetic acid → (2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[1-(4-nitrobenzyloxycarbonyl)-2-imidazolin-2-yl]pyrrolidine

https://huagongshe.com/ko/reaction/37267

반응식

참여 물질

역할이름HCID투입량
반응물Thioacetic acidHCID 10484—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(2S,4R)-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)-2-[1-(4-nitrobenzyloxycarbonyl)-2-imidazolin-2-yl]pyrrolidineHCID 57217669—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[1-(4-nitrobenzyloxycarbonyl)-2-imidazolin-2-yl]pyrrolidineHCID 57030574—

반응 단계

(2S, 4R) -4-Hydroxy-1-(4-nitrobenzyloxycarbonyl)-2-[1-(4-nitrobenzyloxycarbonyl)-2-imidazolin-2-yl]-pyrrolidine (655 mg) and triphenylphosphine (0.51 g) were dissolved in tetrahydrofuran (20 ml) at 0° C. To this solution was added dropwise a solution of diethyl azodicarboxylate (0.30 ml) in tetrahydrofuran (5 ml) with stirring for 30 minutes, followed by addition of a solution of thioacetic S-acid (0.14 ml). Stirring was continued at ambient temperature for 2 hours. The reaction mixture was diluted with ethyl acetate, washed with saturated sodium bicarbonate and brine, dried over magnesium sulfate and evaporated. The obtained oily residue was subjected to a column chromatography on silica gel and eluted with a mixture of dichloromethane and acetone (20:1, V/V) to give (2S, 4S )-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-[1-(4-nitrobenzyloxycarbonyl)-2-imidazolin-2 -yl]-pyrrolidine (1.2 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420122
출처 데이터셋uspto-grants-1995_05
ORD IDord-a0bfcbd3b6614975a651750dcbc5260b
출처 메모uspto-grants-1995_05