Reaktionsgleichung
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]([NH2:12])[CH3:11])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[F:13][C:14]([F:41])([S:37]([OH:40])(=[O:39])=[O:38])[C:15]([F:36])([F:35])[C:16]([F:34])([F:33])[C:17]([F:32])([F:31])[C:18]([F:30])([F:29])[C:19]([F:28])([F:27])[C:20]([F:26])([F:25])[C:21]([F:24])([F:23])[F:22]>C(O)C>[F:41][C:14]([F:13])([S:37]([O-:40])(=[O:39])=[O:38])[C:15]([F:35])([F:36])[C:16]([F:34])([F:33])[C:17]([F:31])([F:32])[C:18]([F:30])([F:29])[C:19]([F:28])([F:27])[C:20]([F:26])([F:25])[C:21]([F:24])([F:23])[F:22].[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]([NH3+:12])[CH3:11])=[CH:6][CH:5]=1)([CH3:3])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The perfluoro-octylsulphonate salt was prepared by mixing a solution of 1-(4-isopropylphenyl)ethylamine (16.1 g) in ethanol (20 ml) with a solution of perfluoro-octylsulphonic acid (50 ml). The solution was evaporated to dryness and the residue was recrystallised from chloroform as soft colourless plates of 1-(4-isopropylphenyl) ethyl ammonium perfluoro-octyl sulphonate, melting point 158° C.(d). (Found: C 34.3; H 2.5; N 2.2%. C19H18F17NO3S requires: C 34.40; H 2.73; N 2.11%).
Aufarbeitung
- customThe solution was evaporated to dryness
- customthe residue was recrystallised from chloroform as soft colourless plates of 1-(4-isopropylphenyl) ethyl ammonium perfluoro-octyl sulphonate, melting point 158° C.(d)
Quellen und Nachweise
- ORD-Eintrag
- ord-6d585b59466345fe8cd212ca150b32da
- Quelldatensatz
- uspto-grants-1982_09
- Patentnummer
- US04350644
Verknüpfte Notizen
Wird geladen…