Diisopropylethylamine → 1-(2-fluoro-4-nitrophenyl)-4-methyl-1H-imidazole

HRID 723773ノート

反応式

HRID 723773 の反応式
[CH3:1][C:2]1[N:3]=[CH:4][NH:5][CH:6]=1.C(N(CC)C(C)C)(C)C.[F:16][C:17]1[CH:18]=[C:19]([N+:24]([O-:26])=[O:25])[CH:20]=[CH:21][C:22]=1F>C(#N)C>[F:16][C:17]1[CH:18]=[C:19]([N+:24]([O-:26])=[O:25])[CH:20]=[CH:21][C:22]=1[N:5]1[CH:6]=[C:2]([CH3:1])[N:3]=[CH:4]1

参加物

5

反応物 3

HCID 81531DiisopropylethylamineHCID 1230531,2-Difluoro-4-nitrobenzeneHCID 178418800HCID 178418800、化合物

生成物 1

HCID 218765961-(2-fluoro-4-nitrophenyl)-4-methyl-1H-imidazole

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

4-Methylimidazole (45.1 g, 0.55 M) and N,N-diisopropylethylamine (161 g, 1.25 M) were dissolved in acetonitrile (800 ml), and 3,4-difluoronitrobenzene (79.5 g, 0.5 M) added. The mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated, the residue dissolved in ethyl acetate (800 ml), washed with water (400 ml), brine (200 ml), and dried (magnesium sulfate). The residue was dissolved in toluene (250 ml), treated with charcoal, filtered, and diluted with hot cyclohexane (75 ml) to crystallise 3-fluoro-4-(4-methylimidazol-1-yl)nitrobenzene (64.7 g).

後処理

  1. temperatureheated
  2. temperatureto reflux under nitrogen for 24 hours
  3. customSolvent was evaporated
  4. dissolutionthe residue dissolved in ethyl acetate (800 ml)
  5. washwashed with water (400 ml), brine (200 ml)
  6. dry with materialdried (magnesium sulfate)
  7. dissolutionThe residue was dissolved in toluene (250 ml)
  8. additiontreated with charcoal
  9. filtrationfiltered
  10. additiondiluted with hot cyclohexane (75 ml)
  11. customto crystallise 3-fluoro-4-(4-methylimidazol-1-yl)nitrobenzene (64.7 g)

出典と根拠

ORDレコード
ord-ae829dab4e6540e49634f37db63c8f4d
出典データセット
uspto-grants-2006_11
特許番号
US07141583B2

反応ノート

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