Reaktionsgleichung
[F:1][C:2]([F:17])([S:13]([OH:16])(=[O:15])=[O:14])[C:3]([F:12])([F:11])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6].[OH-].[CH2:19]([N+:26]([CH3:29])([CH3:28])[CH3:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:19]([N+:26]([CH3:29])([CH3:28])[CH3:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[F:17][C:2]([F:1])([S:13]([O-:16])(=[O:15])=[O:14])[C:3]([F:11])([F:12])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6]Komponenten
3
Versuchsvorschrift
Perfluorobutanesulfonic acid benzyltrimethylammonium salt is prepared by neutralising perfluorobutanesulfonic acid and benzyltrimethylammonium hydroxide in aqueous solution. Benzyltrimethylammonium hydroxide is obtainable from Aldrich.
Quellen und Nachweise
- ORD-Eintrag
- ord-72007794f9f04d989d5f2583f29f5ba0
- Quelldatensatz
- uspto-grants-2007_01
- Patentnummer
- US07169333B2
Verknüpfte Notizen
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