Methyl iodide → 2-Bromo-3-methoxy-6-methylpyridine

HRID 488814

反応式

HRID 488814 の反応式
[Br:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[C:4]([CH3:9])[N:3]=1.[C:10](=O)([O-])[O-].[K+].[K+].IC>CC(C)=O>[Br:1][C:2]1[C:7]([O:8][CH3:10])=[CH:6][CH:5]=[C:4]([CH3:9])[N:3]=1

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 119591012-Bromo-6-methylpyridin-3-ol

生成物 1

HCID 109655632-Bromo-3-methoxy-6-methylpyridine収率 88.3%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A stirred mixture of 2-bromo-3-hydroxy-6-methyl-pyridine (7.89 g, 42.0 mmol), potassium carbonate (11.60 g, 83.9 mmol) and iodomethane (8.93 g, 62.9 mmol, 3.92 mL) in acetone (100 mL) was heated under reflux overnight. The mixture was filtered, evaporated and purified on silica gel (hexane:ethyl acetate, 95:5 to 9:1) to give the desired product as a white solid (7.49 g, 88.3%). 1H NMR (500 MHz, CDCl3): δ 2.46 (s, 3 H), 3.87 (s, 3 H), 7.04 (s, 2 H).

後処理

  1. temperaturewas heated
  2. temperatureunder reflux overnight
  3. filtrationThe mixture was filtered
  4. customevaporated
  5. custompurified on silica gel (hexane:ethyl acetate, 95:5 to 9:1)

出典と根拠

ORDレコード
ord-58635002450b4ed6aaeee81ac6a86c27
出典データセット
uspto-grants-2005_12
特許番号
US06974826B2

関連ノート

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