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HRID 2079914作成日:2026年10月27日

Iodoethane → 1-Ethyl-2-methyl-6-nitro-1H-indole

https://huagongshe.com/reaction/2079914

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Ethyl AcetateHCID 8857—
反応物2-Methyl-6-nitro-1H-indoleHCID 600508—
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
溶媒DimethylformamideHCID 6228—
生成物1-Ethyl-2-methyl-6-nitro-1H-indoleHCID 57442275100%

反応手順

Cool a solution of 2-methyl-6-nitro-1H-indole, 18 (0.31 g, 1.76 mmol) in anhydrous DMF (5 mL) under inert atmosphere at 0° C. Add sodium hexamethyldisilazide (1.0M in THF, 1.9 mL, 1.9 mmol) and stir 5 minutes. Add iodoethane (filtered through basic alumina) (0.43 mL, 5.28 mmol), warm to ambient temperature, and stir 2 hours. Quench the reaction with saturated aqueous sodium bicarbonate, add ethyl acetate, and wash with saturated aqueous sodium bicarbonate followed by saturated aqueous brine. Dry the organic layer over sodium sulfate, filter, and concentrate in vacuo. Chromatograph over silica gel using hexanes/ethyl acetate (9:1) to afford the title compound, (0.36 g, 100%). 1H NMR (CDCl3, 300 MHz) δ 2.47 (s, 31), 4.18 (q, J=7.1 Hz, 2), 6.23 (s, 3H), 7.48 (d, J=8.8 Hz, 1H), 7.95 (dd, J=1.9, 8.6 Hz, 1H), 8.23 (d, J=1.9 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07932284B2
出典データセットuspto-grants-2011_04
ORD IDord-8c02373d2b1848c2b67e6759d8ead9b2
出典メモuspto-grants-2011_04