Reaktionsgleichung
[CH:1]1[CH:2]=[CH:3][C:4]([C:7]2[N:8]=[C:9]([NH2:14])[N:10]=[C:11]([NH2:13])[N:12]=2)=[CH:5][CH:6]=1.[NH3:15].Cl[S:17]([OH:20])(=O)=[O:18]>>[NH2:13][C:11]1[N:10]=[C:9]([NH2:14])[N:8]=[C:7]([C:4]2[CH:3]=[CH:2][CH:1]=[C:6]([S:17](=[O:20])(=[O:18])[NH2:15])[CH:5]=2)[N:12]=1Komponenten
4
Versuchsvorschrift
6.0 g of benzoguanamine is heated in 30 g of chlorosulfonic acid at 130° to 140° C. for 4 hours. After cooling, the mixture is added dropwise into 300 ml of 28% aqueous ammonia with stirring and after 1 hour, the insoluble matter is filtered out and recrystallized from aqueous dimethylsulfoxide. Melting point: over 290° C.; yield: 2.0 g.
Aufarbeitung
- temperatureAfter cooling
- filtrationthe insoluble matter is filtered out
- customrecrystallized from aqueous dimethylsulfoxide
- customover 290° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-4b370c371aa94fcc940940bdf1d34c7c
- Quelldatensatz
- uspto-grants-1978_07
- Patentnummer
- US04103009
Verknüpfte Notizen
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