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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37268생성일: 2026년 10월 24일

Boron trifluoride etherate → (2S,4S)-4-acetylthio-2-(1,3-dithiolan-2-yl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/ko/reaction/37268

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물1,2-EthanedithiolHCID 10902—
반응물Sodium BicarbonateHCID 516892—
반응물(2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 18638815—
용매DichloromethaneHCID 6344—
생성물(2S,4S)-4-acetylthio-2-(1,3-dithiolan-2-yl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 57182042—

반응 단계

To a solution of (2S,4S)-4-acetylthio-2-formyl-1-(4-nitrobenzyloxycarbonyl) pyrrolidine (1.00 g) and 1,2-ethanedithiol (0.36 ml) in dichloromethane (20 ml) was added boron trifluoride etherate (0.1 ml), and the solution was stirred for 14 hours at ambient temperature. To the mixture was added saturated aqueous sodium hydrogen carbonate and the organic layer was separated, and washed with brine. The organic layer was dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (50 ml) and eluted with a mixture of acetone and dichloromethane (2:98, V/V) to give (2S, 4S)-4-acetylthio-2-(1,3-dithiolan-2-yl) -1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.14 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420122
출처 데이터셋uspto-grants-1995_05
ORD IDord-4ce6fdb16cdc47aeb1dd914270f8e3ab
출처 메모uspto-grants-1995_05