Reaktionsgleichung
[CH3:1][N:2]1[C:6]([CH3:7])=[C:5]([N:8]=O)[C:4](=[O:10])[N:3]1[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH3:17][C:18]1[CH:23]=[CH:22][C:21]([NH2:24])=[CH:20][C:19]=1[NH2:25].[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[Na+]>C(O)(=O)C.O>[Cl:26]([O-:30])(=[O:29])(=[O:28])=[O:27].[NH2:24][C:21]1/[C:22](=[N:8]/[C:5]2[C:4](=[O:10])[N:3]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[N:2]([CH3:1])[C:6]=2[CH3:7])/[CH:23]=[C:18]([CH3:17])[C:19](=[NH2+:25])[CH:20]=1Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
50 mmol of 1,5-dimethyl-4-nitroso-2-phenyl-1,2-dihydro-3H-pyrazol-3-one was dissolved in a solution of 850 ml of acetic acid and 1250 ml of water. This solution was admixed with 50 mmol of 4-methylbenzene-1,3-diamine and stirring was continued for 2 h 30 min. Sodium perchlorate was added to saturation, and the mixture was left to stand for 30 minutes at zero degrees.
Aufarbeitung
- waitthe mixture was left
- waitto stand for 30 minutes at zero degrees
Quellen und Nachweise
- ORD-Eintrag
- ord-337954db342c466cbcef6fe9888bb754
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07582123B2
Verknüpfte Notizen
Wird geladen…