Reaktionsgleichung
[NH2:1][CH2:2][CH:3]1[CH2:8][CH2:7][CH:6]([CH2:9][NH2:10])[CH2:5][CH2:4]1.C(C1C=CC=CC=1C#N)#N>>[NH2:1][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH2:10])=[CH:5][CH:4]=1Komponenten
3
Versuchsvorschrift
It is known to prepare 1,4-bis(aminomethyl)cyclohexane from dicyanobenzene in a two stage process as disclosed, e.g., in DE-A 3,003,730. In the first stage dicyanobenzene is catalytically hydrogenated to produce 1,4-bis(aminomethyl)benzene, which is then catalytically hydrogenated to produce 1,4-bis(aminomethyl)cyclohexane. One disadvantage is that the starting material must be produced with hydrogen cyanide.
Quellen und Nachweise
- ORD-Eintrag
- ord-df5237de56f24ca5928ad22d0782c545
- Quelldatensatz
- uspto-grants-1998_08
- Patentnummer
- US05789620
Verknüpfte Notizen
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