Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37015생성일: 2026년 10월 25일
Dimethylformamide → 3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine
https://huagongshe.com/reaction/37015
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-Methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine | HCID 53997171 | — |
| 반응물 | HCID 178418634 | HCID 178418634 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 3-Acetylthio-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine | HCID 54037145 | 79.1% |
반응 단계
To 300 ml of anhydrous N,N-dimethylformamide were added 7.35 g of sodium hydride in the form of a 55% w/w/ dispersion in oil, followed by 12.5 g of thioacetic acid. The mixture was then stirred for 10 minutes, with ice-cooling, after which 40 g of 3-methanesulphonyloxy-1-(N-p-nitrobenzyloxycarbonylacetimidoyl)pyrrolidine were added. The mixture was then stirred for 3 hours at 65° C. After the reaction mixture had been allowed to cool, water was added and the mixture was extracted with ethyl acetate. The extract was washed with water and dried and then the solvent was distilled off under reduced pressure. The residue was purified by chromatography through a column of silica gel, eluted with a 2:1 by volume mixture of benzene and ethyl acetate, to give 30 g of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | USRE034960 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-10b960678bc34a7c81eff1c395c66e14 |
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| 출처 메모 | uspto-grants-1995_05 |
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