Tetrahydrofuran → HCID 178479811, Verbindung
Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[CH2:8]([N:10](CC)CC)C.[Pt:15]([Cl:19])(Cl)(Cl)[Cl:16].[CH2:20]1[CH2:24][O:23][CH2:22][CH2:21]1>>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[O:1][Pt:15]([Cl:19])([Cl:16])[O:23][C:24]1[CH:20]=[CH:21][CH:22]=[CH:8][N:10]=1Komponenten
5
Versuchsvorschrift
To a solution of 0.02 moles of 2-hydroxypyridine and 0.02 moles of triethylamine in 50 mL of THF, a solution of 0.01 moles of platinum tetrachloride is added dropwise at 0° C. The solution is then stirred overnight at room temperature. After filtration, the THF solution is evaporated and the product is extracted from the residue. Polymers may be produced using the catalyst by following the procedure of Example 4.
Aufarbeitung
- filtrationAfter filtration
- customthe THF solution is evaporated
- extractionthe product is extracted from the residue
- customPolymers may be produced
Quellen und Nachweise
- ORD-Eintrag
- ord-836569bce09a4e0993cbedf0b4c03976
- Quelldatensatz
- uspto-grants-2004_07
- Patentnummer
- US06759493B1
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