1,4-Cyclohexadiene-1,4-dicarboxylic acid, 2,5-bis(phenylamino)-, 1,4-dimethyl ester → Quinacridone
反応式
[NH:1]([C:8]1[CH2:17][C:16]([C:18]([O:20]C)=O)=[C:15]([NH:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:14][C:9]=1[C:10]([O:12]C)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O>[CH:26]1[CH:27]=[C:28]2[C:18]([C:16]3[C:15]([NH:22][C:23]2=[CH:24][CH:25]=1)=[CH:14][C:9]1[C:10]([C:7]2[C:2]([NH:1][C:8]=1[CH:17]=3)=[CH:3][CH:4]=[CH:5][CH:6]=2)=[O:12])=[O:20]参加物
3
実験手順
A suspension of 200 g of dimethyl 2,5-dianilino-3,6-dihydroterephthalate in 1 l of water was introduced by means of a two-material nozzle and 1.5 m3 of nitrogen into a tubular reactor (50 mm in diameter, 300 mm in length) at 395° C. Using a solids filter, 170 g of dihydroquinacridone (purity 95%, includes about 3% of quinacridone) were obtained.
後処理
- additionwas introduced by means of a two-material nozzle and 1.5 m3 of nitrogen into a tubular reactor (50 mm in diameter, 300 mm in length) at 395° C