Reaktionsgleichung
[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]([OH:18])=[CH:4][C:3]=1[O:19][CH3:20].[CH2:21]([C:23]([CH2:28][CH3:29])(CO)[CH2:24][OH:25])[CH3:22].[OH-].[K+]>>[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5]([OH:18])=[CH:4][C:3]=1[O:19][CH2:20][C:23]([CH2:28][CH3:29])([CH2:21][CH3:22])[CH2:24][OH:25]Komponenten
4
Versuchsvorschrift
13 parts of 1-amino-2-methoxy-4-hydroxyanthraquinone, 50 parts of 2,2-diethyl-1,3-propanediol, 2.5 parts of a polyethylene oxide of average molecular weight 200 and 1.5 parts of potassium hydroxide are stirred for 2.5 hours at 160°C under nitrogen. After working up, 10 parts of 1-amino-2-(2',2'-diethyl-3'-hydroxypropanoxy)-4-hydroxyanthraquinone are obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-756f459f53294d70bc6b221497c89255
- Quelldatensatz
- uspto-grants-1976_07
- Patentnummer
- US03968131
Verknüpfte Notizen
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