反応式
[CH3:1][NH:2][C:3]1[C:16]2[C:15](=[O:17])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8](=[O:18])[C:7]=2[C:6](Br)=[CH:5][CH:4]=1.[F:20][C:21]([F:31])([F:30])[O:22][C:23]1[CH:29]=[CH:28][C:26]([NH2:27])=[CH:25][CH:24]=1.C([O-])(=O)C.[K+]>C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:1][NH:2][C:3]1[C:16]2[C:15](=[O:17])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8](=[O:18])[C:7]=2[C:6]([NH:27][C:26]2[CH:28]=[CH:29][C:23]([O:22][C:21]([F:20])([F:30])[F:31])=[CH:24][CH:25]=2)=[CH:5][CH:4]=1参加物
5
反応条件
- 温度
- 132 °C
実験手順
12.64 parts of 1-methylamino-4bromo-anthraquinone, 9.9 parts of para-trifluoromethoxyaniline, 6 parts of potassium acetate and 2 parts of copper acetate are introduced into 43 parts of 4-methyl-2-pertanol and the mixture is heated at 132° C. for 8 hours. The mixture is then cooled to 60° C., filtered, washed with water, then the precipitate is taken up in dilute caustic soda, filtered, washed and dried. 9.6 parts of 1-methylamino-4-(p-trifluoromethoxy-anilino)-anthraquinone are obtained.
後処理
- temperatureThe mixture is then cooled to 60° C.
- filtrationfiltered
- washwashed with water
- filtrationfiltered
- washwashed
- customdried
出典と根拠
- ORDレコード
- ord-ac64c7d594e14581bcbb8eb574d9b28c
- 出典データセット
- uspto-grants-1977_07
- 特許番号
- US04035397
関連ノート
読み込み中…