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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2215780생성일: 2026년 10월 25일

Methyl iodide → 1,5-Dimethyl-7-bromoindole

https://huagongshe.com/reaction/2215780

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물7-Bromo-5-methyl-1H-indoleHCID 3403330—
용매DimethylformamideHCID 6228—
생성물1,5-Dimethyl-7-bromoindoleHCID 2194996296%

반응 단계

To a suspension of sodium hydride (60%, 0.91 g, 22.9 mmol) in DMF (70 mL) was added a solution of 5-methyl-7-bromoindole (4.0 g, 19.05 mmol) in DMF (10 mL). The mixture was stirred at room temperature for 1 h, and then methyl iodide (1.78 mL, 28.6 mmol) was added with cooling in an ice-water-bath. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction was quenched with water and extracted with ethyl acetate. The extract was washed with water and brine, dried (sodium sulfate) and concentrated to give a crude product (4.1 g, 96%), which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 2.38 (s, 3H), 4.12 (s, 3H), 6.36 (d, J=3.12 Hz, 1H), 6.95 (d, J=3.13 Hz, 1H), 7.18 (d, J=1.56 Hz, 1H), 7.31 (dd, J1=0.79 Hz, J2=1.56 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07109229B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-12bc21d35cd446ed8b153ecd0cccc676
출처 메모uspto-grants-2006_09