反応式
[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-])=O)=[CH:7][C:6]=1[CH3:14])[C:2]([CH3:4])=[O:3].[H][H]>[Ni].CN(C)C=O>[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([NH2:11])=[CH:7][C:6]=1[CH3:14])[C:2]([CH3:4])=[O:3]参加物
5
実験手順
19.4g (0.1 mole) of 4-acetamino-3-methyl-nitrobenzene, 30g of dimethylformamide and 1g of fresh-developed Raney nickel were fed in an autoclave, 50kg/cm2 of hydrogen was then fed thereto, and, after the reaction was carried out at 60° to 120° C while stirring, the reaction mixture was removed immediately, the Raney nickel was removed while hot, and thereafter the product was poured into 100ml of methanol to separate the 4-acetamino-3-methylaniline produced.
後処理
- customwas carried out at 60° to 120° C
- customthe reaction mixture was removed immediately
- customthe Raney nickel was removed while hot, and thereafter the product
- additionwas poured into 100ml of methanol
- customto separate the 4-acetamino-3-methylaniline
- customproduced
出典と根拠
- ORDレコード
- ord-1170cedb5a914ef7a9703441e9dbd141
- 出典データセット
- uspto-grants-1977_02
- 特許番号
- US04009205
関連ノート
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