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Imidazole → 3-(1H-imidazol-1-yl)benzonitrile

HRID 619169
ノート
印刷プレビュー

反応式

HRID 619169 の反応式
F[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[C:5]#[N:6].[NH:10]1[CH:14]=[CH:13][N:12]=[CH:11]1.C([O-])([O-])=O.[K+].[K+].[I-].[K+]>[Cu].CN(C=O)C>[N:10]1([C:2]2[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=2)[C:5]#[N:6])[CH:14]=[CH:13][N:12]=[CH:11]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 795ImidazoleHCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 678803-Fluorobenzonitrile

生成物 1

HCID 49612723-(1H-imidazol-1-yl)benzonitrile収率 47.1%

試薬・触媒・溶媒 2

HCID 23978Copper触媒
HCID 6228
Dimethylformamide
溶媒

実験手順

A mixture of 3-fluorobenzonitrile (18 ml, 168.38 mmol), imidazole (11.46 g), K2CO3 (25.59 g), copper (1.75 g), potassium iodide (1.75 g) and DMF (125 ml) was refluxed overnight. The reaction mixture was cooled to room temperature and poured into ice/water (600 ml). A precipitate formed, which was collected by filtration, washed with water, dissolved in ethanol (25 ml)/CHCl3 (500 ml) and filtered. The filtrates were partitioned in water, the organic layer was separated, dried over MgSO4 and stripped. The residue was combined with the product from another experimental run and was recrystallized from CHCl3 /hexanes to afford 13.4 g of 3-(1-imidazolyl)benzonitrile.

後処理

  1. temperaturewas refluxed overnight
  2. customA precipitate formed
  3. filtrationwhich was collected by filtration
  4. washwashed with water
  5. dissolutiondissolved in ethanol (25 ml)/CHCl3 (500 ml)
  6. filtrationfiltered
  7. customThe filtrates were partitioned in water
  8. customthe organic layer was separated
  9. dry with materialdried over MgSO4
  10. customwas recrystallized from CHCl3 /hexanes

出典と根拠

ORDレコード
ord-daf1b6eed2f2433f9e539d87fdd08975
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05958929

反応ノート

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