Reaktionsgleichung
[C:1]1([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:6]=[CH:5][C:4]([S:7]([OH:10])(=[O:9])=[O:8])=[CH:3][CH:2]=1.FC(F)(F)C(O)=O.[N+:24]([O-])([OH:26])=[O:25]>>[N+:24]([C:14]1[CH:15]=[CH:16][C:11]([C:1]2[CH:6]=[CH:5][C:4]([S:7]([OH:10])(=[O:8])=[O:9])=[CH:3][CH:2]=2)=[CH:12][CH:13]=1)([O-:26])=[O:25]Komponenten
4
Reaktionsbedingungen
- Temperatur
- -5 °C
Versuchsvorschrift
Biphenyl-4-sulfonic acid (30 g) was mixed with trifluoroacetic acid and a suspension was formed. The mixture was cooled to −5° C. Fuming nitric acid (12.8 ml) was added dropwise over 30 min. The reaction mixture was stirred at 0° C. for 2 h. The chloroform was removed in vacuo and the residue was recrystallized from acetic acid to provide 15 g of 4′-nitro-biphenyl-4-sulfonic acid, obtained as white crystals.
Aufarbeitung
- customa suspension was formed
- customThe chloroform was removed in vacuo
- customthe residue was recrystallized from acetic acid
Quellen und Nachweise
- ORD-Eintrag
- ord-c85642210abd41d89146536782ef2f01
- Quelldatensatz
- uspto-grants-2008_09
- Patentnummer
- US07420001B2
Verknüpfte Notizen
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