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Methyl iodide → 5-fluoro-6-iodo-1-methyl-1H-indole

HRID 222468
ノート
印刷プレビュー

反応式

HRID 222468 の反応式
[I:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[CH:7][NH:8]2)=[CH:4][C:3]=1[F:11].[H-].[Na+].I[CH3:15]>CN(C=O)C>[F:11][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:2]=1[I:1])[N:8]([CH3:15])[CH:7]=[CH:6]2
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 226127725-fluoro-6-iodo-1H-indole

生成物 1

HCID 685242905-fluoro-6-iodo-1-methyl-1H-indole収率 96.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

To a solution of 6-iodo-5-fluoro-1H-indole (0.495 g, 1.890 mmol) in dry DMF (7.0 mL) was added sodium hydride (55% suspension in oil) (0.124 g, 2.840 mmol) at 0° C. The mixture was stirred at 0° C. for 30 min, and then iodomethane (0.15 mL, 2.47 mmol) was added. The mixture was stirred for 1 hour at room temperature, and then quenched with ice and extracted with EtOAc (50 mL). The organic layer was washed with water, brine, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (EtOAc-hexane, 1:9) to afford 5-fluoro-6-iodo-1-methyl-1H-indole as a colorless solid (0.50 g, 96%).

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. stirringThe mixture was stirred for 1 hour at room temperature
  2. customquenched with ice
  3. extractionextracted with EtOAc (50 mL)
  4. washThe organic layer was washed with water, brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified by column chromatography (EtOAc-hexane, 1:9)

出典と根拠

ORDレコード
ord-a508b61691fa4a808cabed1c880ca87c
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08207216B2

反応ノート

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