Methyl iodide → 1,3-Dimethylindole

HRID 1297358

反応式

HRID 1297358 の反応式
[CH3:1][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1.[H-].[Na+].I[CH3:14]>CN(C=O)C>[CH3:14][N:4]1[C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[C:2]([CH3:1])=[CH:3]1

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 6736SkatoleHCID 24758Sodium hydride

生成物 1

HCID 701301,3-Dimethylindole収率 97.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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, 1H), 7.35 (d, J=8.2 Hz, 1H), 7.13 (t, 1H), 7.06 (s, 1H), 7.00 (t, 1H), 3.71 (s, 3H), 2.24 (s, 3H).

後処理

  1. temperaturewas cooled in an ice bath
  2. waitAfter 16 hr at RT
  3. concentrationthe reaction was concentrated under vacuum
  4. washThe solution was washed with H2O
  5. dry with materialwith brine, dried (MgSO4)
  6. concentrationconcentrated to dryness
  7. customPurification
  8. distillationby short path distillation under vacuum (bp 88-92° C., 0.5 mmHg)

出典と根拠

ORDレコード
ord-4f906dfd221542158da74d186df654d1
出典データセット
uspto-grants-2007_07
特許番号
US07250424B2

関連ノート

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