Reaktionsgleichung
[F:1][B-:2]([F:5])([F:4])[F:3].[H+].[N:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>>[F:1][B-:2]([F:5])([F:4])[F:3].[NH+:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Komponenten
3
Versuchsvorschrift
Tetrafluoroboric acid (250 ml, 2.00 mol) was added to cool (0° C.) pyridine (157.7 ml, 1.95 mol) and within 25 min a colorless precipitate was obtained. After the acid was completely added the mixture was further stirred for 30 min at the same temperature. Then the reaction mixture was filtered. The residue was washed twice with cold ethanol and dried 12 h at high vacuum to yield 201.9 g (60%) pyridiniumtetrafluoroborate as colorless crystals.
Aufarbeitung
- customwithin 25 min a colorless precipitate was obtained
- additionAfter the acid was completely added the mixture
- filtrationThen the reaction mixture was filtered
- washThe residue was washed twice with cold ethanol
- customdried 12 h at high vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-2276f2b332ac44709ebb2e2b240805ef
- Quelldatensatz
- uspto-grants-2015_07
- Patentnummer
- US09085535B2
Verknüpfte Notizen
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