Reaktionsgleichung
N[C:2]1[CH:11]=[C:10](S(O)(=O)=O)[CH:9]=[C:8]2[C:3]=1[C:4]([OH:20])=[CH:5][C:6](S(O)(=O)=O)=[CH:7]2.ClC1N=C(Cl)N=C(Cl)N=1.NC1C=CC=CC=1>>[CH:10]1[CH:11]=[CH:2][C:3]2[C:8](=[CH:7][CH:6]=[CH:5][C:4]=2[OH:20])[CH:9]=1Komponenten
4
Versuchsvorschrift
In an aqueous solvent, 31.9 parts of 5-amino-4-hydroxynaphthalene-2,7-disulfonic acid was condensed with 18.4 parts of 2,4,6-trichloro-s-triazine according to a normal method and the resultant condensate was condensed with 28.1 parts of 3-(2-sulfate ethylsulfonyl)aniline according to a normal method. The product thus obtained was condensed with 9.3 parts of aniline according to a normal method to obtain a naphthol derivative.
Aufarbeitung
- customThe product thus obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-b54a03377a9d4d37853de6453c6ef1ab
- Quelldatensatz
- uspto-grants-2000_01
- Patentnummer
- US06015885
Verknüpfte Notizen
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