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HRID 18229作成日:2026年10月23日

Methyl iodide → 1,3-Dimethylindole

https://huagongshe.com/ja/reaction/18229

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SkatoleHCID 6736—
反応物Sodium hydrideHCID 24758—
溶媒DimethylformamideHCID 6228—
生成物1,3-DimethylindoleHCID 7013097.3%

反応手順

To a stirred solution of 3-methylindole (15.0 g, 114 mmole) in dry DMF (200 mL) was added NaH (60% dispersion in oil, 5.0 g, 125 mmole) in portions. Gas evolution was observed. The mixture was stirred for 30 min, then iodomethane (8 mL, 129 mmole) was added in one portion. The reaction became exothermic and was cooled in an ice bath. After 16 hr at RT, the reaction was concentrated under vacuum and the residue was taken up in ethyl acetate. The solution was washed with H2O then with brine, dried (MgSO4), and concentrated to dryness. Purification by short path distillation under vacuum (bp 88-92° C., 0.5 mmHg) gave the title compound (16.10 g, 97%) as a pale yellow oil: 1H NMR (400 MHz, CDCl3) δ 7.47 (d, J=7.9 Hz, 1 H), 7.35 (d, J=8.2 Hz, 1 H), 7.13 (t, 1 H), 7.06 (s, 1 H), 7.00 (t, 1 H), 3.71 (s, 3 H), 2.24 (s, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741339B2
出典データセットuspto-grants-2010_06
ORD IDord-ae30e185857c41568a036fdf7a342e0b
出典メモuspto-grants-2010_06