2-Chloro-4-(trifluoromethyl)benzonitrile → (2-Chloro-4-(trifluoromethyl)phenyl)methanamine
反応式
[Cl:1][C:2]1[CH:9]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]>[Ni].N>[Cl:1][C:2]1[CH:9]=[C:8]([C:10]([F:11])([F:12])[F:13])[CH:7]=[CH:6][C:3]=1[CH2:4][NH2:5]参加物
4
実験手順
A suspension of 1.000 g (4.865 mmol) 2-chloro-4-trifluoromethyl-benzonitrile and 100 mg Raney nickel in conc. methanolic ammonia was hydrogenated for 20 h at RT and 3 bar. The catalyst was filtered off and the filtrate was evaporated down i. vac.
後処理
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated down i
出典と根拠
- ORDレコード
- ord-369bffa514c541d2813c2284a501fb99
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351719B2
反応ノート
読み込み中…