반응식
[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>CN(C)C=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]참가 물질
3
실험 절차
Using a Venturi nozzle, per hour a solution of 300 g of dimethyl 2,5-dianilino-3,6-dihydroterephthalate and 400 ml of N,N-dimethylformamide was nozzled into a preheated gas stream of nitrogen (1.2 m3 /h) and air (300 l/h) at 500° C. This gas-liquid mixture was introduced tangentially into a tubular reactor (50 mm in diameter, 400 mm in length) at 575° C. A conventional workup gave 224 g of crude quinacridone per hour of 98% purity (according to UV).
후처리
- additionThis gas-liquid mixture was introduced tangentially into a tubular reactor (50 mm in diameter, 400 mm in length) at 575° C
출처 및 근거
- ORD 기록
- ord-dd41ef34e77f42d4b3da291433e54769
- 출처 데이터셋
- uspto-grants-1990_09
- 특허 번호
- US04956464
연결된 노트
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