Reaktionsgleichung
CC1C=NC(C)=CN=1.CN([CH2:12][CH2:13][C:14]1[CH:19]=[N:18][C:17]([CH2:20][CH2:21]N(C)C)=[CH:16][N:15]=1)C>>[CH:13]([C:14]1[CH:19]=[N:18][C:17]([CH:20]=[CH2:21])=[CH:16][N:15]=1)=[CH2:12]Komponenten
3
Versuchsvorschrift
The procedure of Example 1 was followed using 2,5-dimethylpyrazine as the starting material. The intermediate, 2,5-bis(N,N-dimethylaminoethyl)pyrazine, was prepared at a yield of 47% (118°-130° C./1.2 mm Hg). The product 2,5-divinylpyrazine was collected at 46°-50° C./1.2 mm Hg (36%, nD =1.595). It was found to be slightly soluble in water. 1H NMR (CDCl3) δ 5.57 (2H, dd, J=9.0, 1.2 Hz), 6.31 (2H, dd, J=17.7, 1.2 Hz), 6.80 (2H, dd, J=17.7, 9.0 Hz), 8.51 (2H, s); 13C NMR (CDCl3) δ 120.18, 133.27, 142.31, 149.38.
Aufarbeitung
- customThe product 2,5-divinylpyrazine was collected at 46°-50° C./1.2 mm Hg (36%, nD =1.595)
Quellen und Nachweise
- ORD-Eintrag
- ord-4af259165735477fa8758f9830fd3531
- Quelldatensatz
- uspto-grants-1995_08
- Patentnummer
- US05439950
Verknüpfte Notizen
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