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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569043생성일: 2026년 10월 24일

Ethenamine, N,N-dimethyl-2-nitro- → 4-Ethoxycarbonyl-3-(2-nitrovinyl)indole

https://huagongshe.com/ko/reaction/569043

반응식

참여 물질

역할이름HCID투입량
반응물Ethenamine, N,N-dimethyl-2-nitro-HCID 518458—
반응물Ethyl indole-4-carboxylateHCID 605034—
용매2,2,2-Trifluoroethyl AcetateHCID 136256—
생성물4-Ethoxycarbonyl-3-(2-nitrovinyl)indoleHCID 54059630—

반응 단계

5 g of 4-ethoxycarbonyl indole are added to a solution of 3.1 g of dimethylamino-2-nitroethylene in 20 ml of trifluoroethyl acetate refrigerated under argon. The reaction mixture is introduced into ice water after it had been standing overnight at room temperature. The aqueous phase is repeatedly extracted with ethyl acetate. The combined ethyl acetate extracts are extracted first with sodium bicarbonate solution, then a saturated sodium chloride solution, dried and evaporated. The residue is recrystallized from ethanol. Yield: 4.5 g of 4-ethoxycarbonyl-3-(2-nitrovinyl)-indole. Yellow crystals with a 197°-199° C. melting point.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04731358
출처 데이터셋uspto-grants-1988_03
ORD IDord-6f2a0ddab3ef4b25b66fd79945d51302
출처 메모uspto-grants-1988_03