Reaktionsgleichung
[CH2:1]1[CH:6]([CH2:7][CH:8]2[CH2:13][CH2:12][CH:11]([NH2:14])[CH2:10][CH2:9]2)[CH2:5][CH2:4][CH:3]([NH2:15])[CH2:2]1.[C:16](=[O:27])([O:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])N.N>>[CH2:19]([O:18][C:16]([NH:15][CH:3]1[CH2:2][CH2:1][CH:6]([CH2:7][CH:8]2[CH2:13][CH2:12][CH:11]([NH:14][C:16]([O:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])=[O:27])[CH2:10][CH2:9]2)[CH2:5][CH2:4]1)=[O:27])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]Komponenten
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
Agitated in a reaction vessel are 210 parts of 4,4'-diaminodicyclohexylmethane with 360 parts of O-octyl carbamate and 150 parts of n-octanol-(1) at a reflux temperature of 185° C.-205° C. for 2 hours while the ammonia is removed by means of distillation. At this point, an additional 650 parts of n-octanol are allowed to flow into the reaction mixture and the reaction is continued at reflux temperature for 10 hours. The reaction mixture, which has been cooled to 100° C., is filtered, and the product is allowed to crystallize by cooling the filtrate. By filtration, washing with octanol and drying, 468 parts of bis(4-octoxycarbonylaminocyclohexyl)methane, C31H58N2O4 (molecular weight 522) are obtained corresponding with 89.6 percent theory relative to 4,4'-bisaminodicyclohexylmethane. The melting point is 129° C.-130° C.
Aufarbeitung
- customat a reflux temperature of 185° C.-205° C.
- customfor 2 hours
- customis removed by means of distillation
- temperatureat reflux temperature for 10 hours
- filtrationis filtered
- customto crystallize
- temperatureby cooling the filtrate
- filtrationBy filtration
- washwashing with octanol
- customdrying
Quellen und Nachweise
- ORD-Eintrag
- ord-67ea79eddd204a538f2800a67b2c474a
- Quelldatensatz
- uspto-grants-1985_02
- Patentnummer
- US04497963
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