Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845231생성일: 2026년 10월 25일
4-Methoxy-3-hydroxy-2-nitrobutyric acid ethyl ester → 3-(4-Acetoxymethylindol-3-yl)-2-nitro-4-methoxy-butyric acid ethyl ester
https://huagongshe.com/reaction/845231
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methoxy-3-hydroxy-2-nitrobutyric acid ethyl ester | HCID 13133986 | — |
| 반응물 | 4-Acetoxymethylindole | HCID 20132383 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 3-(4-Acetoxymethylindol-3-yl)-2-nitro-4-methoxy-butyric acid ethyl ester | HCID 54293572 | — |
반응 단계
4-Acetoxymethylindole (189 g) is dissolved in a mixture of toluene (6 l) and acetic acid (0.7 l). To this solution is added 3-hydroxy-2-nitro-5-oxa-hexanoic acid ethyl ester (570 ml). The flask containing the mixture is evacuated by means of a water jet pump. Then balancing to normal pressure is brought about by argon. Evacuation and pressure balancing are repeated four times. Then the reaction mixture is refluxed for two hours in a water-free argon atmosphere. After concentrating to 2 l the solution is diluted with ethyl acetate and shaken out three times with a liter of 1N hydrochloric acid each. Then it is washed to neutrality with saturated hydrochloric acid solution. The solution, dried over sodium sulfate, is evaporated. The residue is chromatographed on silica gel with dichloromethane. 393 g of the title compound is obtained in oily form.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04757070 |
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| 출처 데이터셋 | uspto-grants-1988_07 |
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| ORD ID | ord-a457c7c2d7da4d5f830c81a6a2ff9ef6 |
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| 출처 메모 | uspto-grants-1988_07 |
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