Chloroform → 1H-Benzimidazol-6-amine,1,2-dimethyl-(9CI)
反応式
O.O.[Sn](Cl)Cl.[CH3:6][N:7]1[C:11]2[CH:12]=[C:13]([N+:16]([O-])=O)[CH:14]=[CH:15][C:10]=2[N:9]=[C:8]1[CH3:19].C(Cl)(Cl)Cl.[OH-].[Na+]>Cl>[CH3:6][N:7]1[C:11]2[CH:12]=[C:13]([NH2:16])[CH:14]=[CH:15][C:10]=2[N:9]=[C:8]1[CH3:19]参加物
6
実験手順
To a stirred solution of tin (II) chloride dihydrate (4.7 g) in concentrated hydrochloric acid (15 ml) was added 1,2-dimethyl-6-nitro-1H-benzimidazole (1 g) (J. Chem. Soc., 1931, 1143-1153), and the mixture was stirred at room temperature for 6 h. The mixture was poured onto ice and chloroform, and basified to pH 10 by the addition of 10M sodium hydroxide solution. The mixture was extracted several times with chloroform and the combined organic extracts dried and concentrated in vacuo to give a brown solid. This was crystallised from ethanol to give the title compound.
後処理
- extractionThe mixture was extracted several times with chloroform
- customthe combined organic extracts dried
- concentrationconcentrated in vacuo
- customto give a brown solid
- customThis was crystallised from ethanol
出典と根拠
- ORDレコード
- ord-1d567858b77f4458823582723d8c69dc
- 出典データセット
- uspto-grants-2009_08
- 特許番号
- US07572915B2
反応ノート
読み込み中…