HCID 3432930、化合物 → 2-(2-Chlorophenoxy)aniline
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N+:15]([O-])=O.[H][H]>O1CCCC1.[Ni]>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[NH2:15]参加物
5
実験手順
A solution of 2-chloro-(2-nitrophenoxy)benzene (5.00 g) in tetrahydrofuran (100 mL) was shaken in a Parr Hydrogenator over Raney nickel at 5 psi hydrogen at room temperature for 4 hours. The catalyst was filtered from the reaction, and the solution was evaporated under vacuum to a yellowish oil which crystallized on standing. The solid was crushed, suspended in hexane and filtered to yield the title compound as a light orange solid. Mp: 44°-45° C.
後処理
- filtrationThe catalyst was filtered from the reaction
- customthe solution was evaporated under vacuum to a yellowish oil which
- customcrystallized
- customThe solid was crushed
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-f4acf4c2855346cbaf1898ef75fb031c
- 出典データセット
- uspto-grants-1994_04
- 特許番号
- US05304644
反応ノート
読み込み中…