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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 403413생성일: 2026년 10월 23일

Ethanol → (2S,4R)-2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidinium chloride

https://huagongshe.com/ko/reaction/403413

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Acetyl chlorideHCID 6367—
반응물(2S,4R)-tert-butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidine-1-carboxylateHCID 59165437—
용매Ethyl AcetateHCID 8857—
생성물(2S,4R)-2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidinium chlorideHCID 86664339102.3%

반응 조건

온도15 °C

반응 단계

To a stirring solution of ethanol at 0° C., was added acetyl chloride (1.77 kg). The resulting solution was aged for 30 min. (2S,4R)-tert-Butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidine-1-carboxylate (2.34 kg) was then added as a solution in EtOAc (8.36 kg) to the acidic ethanol slurry solution at 10° C. The reaction was allowed to proceed for 1 h at 10° C., warmed to 15° C., held at that temperature for 1 h and then warmed to 20° C. After 18 h, EtOAc (8.35 kg) was added to the reactor and the resulting slurry was filtered. The cake was rinsed with EtOAc (8.35 kg) that had been cooled to 0° C. The title compound was placed in a vacuum oven, at 40° C., to remove residual solvent (2.1 kg, 100% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748374B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-f5cff39e98bd4ad0ad2d6a2f5a00ea7d
출처 메모uspto-grants-2014_06