Reaktionsgleichung
[C:1]([NH:5][CH2:6][C:7]1[C:8](=[O:19])[O:9][C:10]2[C:15]([C:16]=1[CH3:17])=[CH:14][CH:13]=[C:12]([OH:18])[CH:11]=2)(=[O:4])[CH:2]=[CH2:3].[C:20]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])(=[O:24])[C:21]([CH3:23])=[CH2:22].N(C(C)(C)C#N)=NC(C)(C)C#N>CN(C)C=O>[C:1]([NH:5][CH2:6][C:7]1[C:8](=[O:19])[O:9][C:10]2[C:15]([C:16]=1[CH3:17])=[CH:14][CH:13]=[C:12]([OH:18])[CH:11]=2)(=[O:4])[CH:2]=[CH2:3].[C:20]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH3:43])(=[O:24])[C:21]([CH3:23])=[CH2:22]Komponenten
5
Versuchsvorschrift
Into a 50 ml flask provided with a condenser, a nitrogen led in tube and an agitator, there are introduced 1 g of acrylamido methyl 7-hydroxy-4-methyl coumarin, 2 g of stearyl methacrylate, 0.3 g of azobis-isobutyronitrile and 6 g of dimethylformamide.
Aufarbeitung
- customInto a 50 ml flask provided with a condenser
- customa nitrogen led in tube
Quellen und Nachweise
- ORD-Eintrag
- ord-095036f637844430aed6ef6a7890c047
- Quelldatensatz
- uspto-grants-1979_08
- Patentnummer
- US04166109
Verknüpfte Notizen
Wird geladen…