Reaktionsgleichung
[CH3:1][C:2]([N:16]=[C:17]=[O:18])([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([N:13]=[C:14]=[O:15])([CH3:12])[CH3:11])[CH:5]=1)[CH3:3].[CH2:19]([NH2:31])[CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][OH:30]>>[CH3:3][C:2]([N:16]=[C:17]=[O:18])([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([N:13]=[C:14]=[O:15])([CH3:11])[CH3:12])[CH:5]=1)[CH3:1].[CH2:19]([NH2:31])[CH2:20][O:21][CH2:22][CH2:23][O:24][CH2:25][CH2:26][O:27][CH2:28][CH2:29][OH:30]Komponenten
3
Versuchsvorschrift
To a one-liter 3-necked flask equipped with a thermometer, stirrer, dropping funnel and a nitrogen inlet was 122 g (0.5M) of TMXDI (from American Cyanamid). Then 193 g (1.0 mole) of tetraethylene glycol monoamine was added over a 50 minute period keeping the temperature below 36° C. A clear viscous product was obtained.
Aufarbeitung
- customTo a one-liter 3-necked flask equipped with a thermometer, stirrer
- customthe temperature below 36° C
- customA clear viscous product was obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-cc123ef2ccd84e13a0072d2a80df34b2
- Quelldatensatz
- uspto-grants-1991_07
- Patentnummer
- US05030754
Verknüpfte Notizen
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