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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569078생성일: 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/569078

반응식

참여 물질

역할이름HCID투입량
반응물4-Methoxy-3-hydroxy-2-nitrobutyric acid ethyl esterHCID 13133986—
반응물4-AcetoxymethylindoleHCID 20132383—
용매Acetic AcidHCID 176—
용매TolueneHCID 1140—
생성물3-(4-Acetoxymethylindol-3-yl)-2-nitro-4-methoxy-butyric acid ethyl esterHCID 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 dicloromethane. 393 g of the title compound is obtained in oily form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731365
출처 데이터셋uspto-grants-1988_03
ORD IDord-28aff600685b425abcbf35c0ea92f9de
출처 메모uspto-grants-1988_03