反应详情

To a suspension of sodium hydride (60%, 0.32 g, 7.96 mmol) in DMF (18 mL) was added a solution of 5-methoxy-7-bromoindole (1.5 g, 6.63 mmol) in DMF (25 mL). The mixture was stirred at room temperature for 1 h, and then methyl iodide (0.62 mL, 9.95 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 (1.6 g, 100%), which was used without further purification. 1HNMR (400 MHz, CDCl3) 3.82 (s, 3H), 4.10 (s, 3H), 6.36 (d, J=3.13 Hz, 1H), 6.96 (d, J=2.74 Hz, 1H), 7.0 (d, J=2.35 Hz, 1H), 7.03 (d, J=2.35 Hz, 1H); MS (ES, m/z): C10H10BrNO: 240.08 (M+(79Br)+1), 242.1 (M+(81Br)+1).

1. temperaturewith cooling in an ice-water-bath
2. temperatureto warm to room temperature
3. stirringstirred overnight
4. customThe reaction was quenched with water
5. extractionextracted with ethyl acetate
6. washThe extract was washed with water and brine
7. dry with materialdried (sodium sulfate)
8. concentrationconcentrated