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HRID 569043作成日:2026年10月26日

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

https://huagongshe.com/reaction/569043

反応式

関与物質

役割名称HCID仕込み量
反応物Ethenamine, N,N-dimethyl-2-nitro-HCID 518458—
反応物Ethyl indole-4-carboxylateHCID 605034—
溶媒2,2,2-Trifluoroethyl AcetateHCID 136256—
生成物4-Ethoxycarbonyl-3-(2-nitrovinyl)indoleHCID 54059630—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04731358
出典データセットuspto-grants-1988_03
ORD IDord-6f2a0ddab3ef4b25b66fd79945d51302
出典メモuspto-grants-1988_03