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HRID 11399作成日:2026年10月24日

Ethenamine, N,N-dimethyl-2-nitro- → (E)-5-Chloro-2-ethyl-3-(2-nitroethenyl)-1H-indole

https://huagongshe.com/ja/reaction/11399

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5-chloro-2-ethyl-1H-indoleHCID 20517175—
溶媒Trifluoroacetic acidHCID 6422—
溶媒Diethylether ethylacetateHCID 21584169—
生成物(E)-5-Chloro-2-ethyl-3-(2-nitroethenyl)-1H-indoleHCID 21974279—

反応手順

The indole 3 (5 mmol) was added to a stirred ice-cooled solution of 1-(dimethylamino)-2-nitroethylene (0.58 g, 5 mmol) in trifluoroacetic acid (5 mL). The mixture was stirred at room temperature under N2, for 0.5 h and then poured onto ice water. The aqueous solution was extracted with ethyl acetate, the combined organic layers were washed with a saturated NaHCO3 solution and then with water. After drying over Na2SO4, the solvent was evaporated under reduced pressure to give a crude orange solid which was suspended in a mixture of EtOAc-Et2O and filtered, or chromatographed on silica gel (cyclohexane/EtOAc, 1:1, as eluent).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098233B2
出典データセットuspto-grants-2006_08
ORD IDord-fd5736776b90490195ef7a703ff54b79
出典メモuspto-grants-2006_08