Reaktionsgleichung
[CH3:1][C:2]1([CH3:9])[CH2:7][CH:6]([CH3:8])[NH:5][CH2:4][NH:3]1.[H][H]>[Ni]>[CH3:1][C:2]1([CH3:9])[CH2:7][CH:6]([CH3:8])[N:5]=[CH:4][NH:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Anal. Calc.ed for C7H16N2 : N, 21.85. Found: N, 21.6 Nuclear magnetic resonance spectrum, solvent CDCl3, δ in ppm; 3.82 s, 2H; 2.87 m, 1H; 1.42 & 1.65, 2d's, 2H; 1.02 d, 3H; 1.08 & 1.13 2s's, 6H; 1.67 s, 2H exchangeable with D2O. A sample of 12.8 grams of 4,4,6-trimethylhexahydropyrimidine and 0.5 grams of 60% nickel catalyst on kieselguhr was heated for 8 hrs. at 185°-187° C. During this time the theoretical amount of hydrogen gas was evolved.
Aufarbeitung
- custom3.82 s, 2H
- custom1.02 d, 3H
- custom1.67 s, 2H exchangeable
- customat 185°-187° C
Quellen und Nachweise
- ORD-Eintrag
- ord-06097486185a4171909bcd2c5113cdf1
- Quelldatensatz
- uspto-grants-1980_07
- Patentnummer
- US04212843
Verknüpfte Notizen
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