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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2079914생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2079914

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Ethyl AcetateHCID 8857—
반응물2-Methyl-6-nitro-1H-indoleHCID 600508—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매DimethylformamideHCID 6228—
생성물1-Ethyl-2-methyl-6-nitro-1H-indoleHCID 57442275100%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07932284B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-8c02373d2b1848c2b67e6759d8ead9b2
출처 메모uspto-grants-2011_04