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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | (2S,4R)-tert-butyl 2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidine-1-carboxylate | HCID 59165437 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | (2S,4R)-2-((1R,2S)-1-(ethoxycarbonyl)-2-vinylcyclopropylcarbamoyl)-4-(4-nitrobenzoyloxy)pyrrolidinium chloride | HCID 86664339 | 102.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08748374B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-f5cff39e98bd4ad0ad2d6a2f5a00ea7d |
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| 출처 메모 | uspto-grants-2014_06 |
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