Reaktionsgleichung
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)(=[O:4])=[O:3].[N+:11]([O-])([OH:13])=[O:12].C(=O)(O)[O-].[Na+]>>[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([N+:11]([O-:13])=[O:12])[CH:6]=1)(=[O:4])=[O:3]Komponenten
4
Versuchsvorschrift
Phenyl methyl sulphone (4.0 g) was added, portionwise, to fuming nitric acid stirred at 0° C. The reaction mixture was allowed to warm to room temperature, stirred for 1 hour, and then poured carefully onto ice. The solution was carefully neutralised with sodium bicarbonate and the mixture filtered at the pump. The solid collected was washed with water and dried under reduced pressure over potassium hydroxide to give the title compound as a white solid (5.63 g) in a sufficient state of purity for the next reaction.
Aufarbeitung
- additionpoured carefully onto ice
- filtrationthe mixture filtered at the pump
- customThe solid collected
- washwas washed with water
- dry with materialdried under reduced pressure over potassium hydroxide
Quellen und Nachweise
- ORD-Eintrag
- ord-4f46a697ee1449fb83383b349f6ca7b4
- Quelldatensatz
- uspto-grants-1999_01
- Patentnummer
- US05856273
Verknüpfte Notizen
Wird geladen…