Reaktionsgleichung
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:12]([OH:15])(=[O:14])=[O:13])[CH:10]=2)[C:5]([S:16]([OH:19])(=[O:18])=[O:17])=[CH:4][CH:3]=1.[NH3:20]>O>[NH2:20][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:12]([OH:15])(=[O:14])=[O:13])[CH:10]=2)[C:5]([S:16]([OH:19])(=[O:18])=[O:17])=[CH:4][CH:3]=1.[NH2:20][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:12]([OH:15])(=[O:14])=[O:13])[CH:10]=2)[CH:5]=[CH:4][CH:3]=1Komponenten
5
Edukt 2
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Process of claim 1 wherein 1-aminonaphthalene-4,7-disulphonic acid is prepared from 1-chloronaphthalene-4,7-disulphonic acid at temperatures below 220° C, and then the temperature of the reaction mixture is raised to 220° to 350° C in the presence of ammonia and water so as to obtain 1-aminonaphthalene-7-sulphonic acid.
Quellen und Nachweise
- ORD-Eintrag
- ord-1b0a964716db4c25ab1aa8cf432215f9
- Quelldatensatz
- uspto-grants-1978_05
- Patentnummer
- US04091013
Verknüpfte Notizen
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