Formic Acid → 5-Methoxy-4-methylbenzimidazole
反応式
[CH3:1][O:2][C:3]1[C:4]([CH3:11])=[C:5]([NH2:10])[C:6]([NH2:9])=[CH:7][CH:8]=1.[CH:12](O)=O>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[NH:9][CH:12]=[N:10][C:5]=2[C:4]=1[CH3:11]参加物
3
反応条件
- 温度
- 60 °C
実験手順
A mixture of 4-methoxy-3-methyl-l,2-benzenediamine (2.8 g, 18A mmol) and formic acid (30 mL) was heated at 60° C. for 30 minutes. The formic acid was removed under reduced pressure and the product was partitioned between chloroform and water containing sufficient sodium hydroxide to basify the solution. After evaporation of the solvent the crude product was chromatographed (methanol:chloroform) to give 2.55 g (84%) of 5-methoxy-4-methyl-1H-benzimidazole.
後処理
- customThe formic acid was removed under reduced pressure
- customthe product was partitioned between chloroform and water containing sufficient sodium hydroxide
- customAfter evaporation of the solvent the crude product
- customwas chromatographed (methanol:chloroform)
出典と根拠
- ORDレコード
- ord-6be311e07a5947c88132b29c86c14593
- 出典データセット
- uspto-grants-1995_07
- 特許番号
- US05436240
反応ノート
読み込み中…