反応式
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH2:7].[C:9]([CH2:11][C:12](OCC)=O)#[N:10]>C(OCCC)(=O)C>[N:7]1[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[NH:8][C:12]=1[CH2:11][C:9]#[N:10]参加物
4
実験手順
Benzimidazole-2-acetonitrile was prepared as follows. A mixture of o-phenylenediamine (1 mole) and ethyl cyanoacetate (2 moles) was refluxed for about 30 hours, cooled, diluted with propyl acetate (225 mL), filtered, washed and dried, to provide benzimidazole-2-acetonitrile in a 60-70% yield. Benzimidazole-2-acetonitrile is also available commercially from Aldrich Chemical Company.
後処理
- customBenzimidazole-2-acetonitrile was prepared
- temperaturewas refluxed for about 30 hours
- temperaturecooled
- filtrationfiltered
- washwashed
- customdried
出典と根拠
- ORDレコード
- ord-a970094587af454482a0d3fad6c612f0
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06169185A
関連ノート
読み込み中…