(Trimethoxysilylpropyl)ethylenediamine → N-Octadecyl-N'-2-(3-Trimethoxysilylpropylamino)Ethyl Urea
Reaktionsgleichung
[NH2:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][CH2:7][Si:8]([O:13][CH3:14])([O:11][CH3:12])[O:9][CH3:10].[CH2:15]([N:33]=[C:34]=[O:35])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]>>[CH2:15]([NH:33][C:34]([NH:1][CH2:2][CH2:3][NH:4][CH2:5][CH2:6][CH2:7][Si:8]([O:13][CH3:14])([O:9][CH3:10])[O:11][CH3:12])=[O:35])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32]Komponenten
3
Versuchsvorschrift
To 22.2 g (0.10 mole) of 3-(2-aminoethylamino)propyltrimethoxysilane under nitrogen was added 29.5 g (0.10 mole) of octadecylisocyanate over a 45 min. period. The reaction temperature rose to ca. 70° C. Upon cooling to ambient temperature, the product solidified to a white wax. IR (neat film) 3300, 2900, 1620, 1570, 1470, 1090 cm-1. NMR (CDCl3) 0.4-1.0 (m; 5H), 1.1-2.0 (m; 34H), 2.4-2.8 (m; 2H), 2.9-3.4 (m; 7H), 3.55 (s; 9H), 5.5 (br s; 2H) ppm.
Aufarbeitung
- customrose to ca. 70° C
Quellen und Nachweise
- ORD-Eintrag
- ord-a47a57bef6b24049b0d31ed4c1e82495
- Quelldatensatz
- uspto-grants-1987_02
- Patentnummer
- US04645846
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