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HRID 2215780作成日:2026年10月26日

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

https://huagongshe.com/reaction/2215780

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物7-Bromo-5-methyl-1H-indoleHCID 3403330—
溶媒DimethylformamideHCID 6228—
生成物1,5-Dimethyl-7-bromoindoleHCID 2194996296%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07109229B2
出典データセットuspto-grants-2006_09
ORD IDord-12bc21d35cd446ed8b153ecd0cccc676
出典メモuspto-grants-2006_09