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2-Methylimidazole → 4-(2-Methyl-1H-imidazol-1-yl)benzaldehyde

HRID 1291044
ノート
印刷プレビュー

反応式

HRID 1291044 の反応式
[H-].[Na+].[CH3:3][C:4]1[NH:5][CH:6]=[CH:7][N:8]=1.F[C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=1>CN(C=O)C>[CH3:3][C:4]1[N:5]([C:10]2[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=2)[CH:6]=[CH:7][N:8]=1
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 127492-MethylimidazoleHCID 24758Sodium hydrideHCID 680234-Fluorobenzaldehyde

生成物 1

HCID 31596624-(2-Methyl-1H-imidazol-1-yl)benzaldehyde収率 35.8%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

反応条件

温度
10 °C

実験手順

To a suspension of NaH (0.612 g, 15.3 mmol : 60% suspension of mineral oil) of in dry DMF (10 ml) cooled to 10° C. was added a DMF (8 ml) solution of 2-methylimidazole (1.23 g, 15 mmol) under a nitrogen atmosphere, and the mixture was stirred for 30 min at room temperature. 4-Fluorobenzaldehyde (1.90 g, 15.3 mmol) was added to the reaction mixture, and the resulting solution was stirred for 14 h. The reaction mixture was poured into an ice-cold saturated aqueous NH4Cl solution (100 ml) and extracted with ethyl acetate (100 ml×2). The organic layer was washed with water (100 ml) and brine (80 ml), dried over MgSO4 and the solvent removed under reduced pressure. The resultant residue was purified by column chromatography (SiO2 ; hexane:ethyl acetate=1:1 then ethyl acetate) to give crude 4-(2-methylimidazol-1-yl)-benzaldehyde (1.0 g), which was used without further purification.

後処理

  1. stirringthe resulting solution was stirred for 14 h
  2. extractionextracted with ethyl acetate (100 ml×2)
  3. washThe organic layer was washed with water (100 ml) and brine (80 ml)
  4. dry with materialdried over MgSO4
  5. customthe solvent removed under reduced pressure
  6. customThe resultant residue was purified by column chromatography (SiO2

出典と根拠

ORDレコード
ord-083e4b7aaf344ee7a67681396c9378a1
出典データセット
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05753682

反応ノート

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