Reaktionsgleichung
[CH2:1]([NH:3][C:4]1[CH:5]=[C:6]([OH:11])[CH:7]=[CH:8][C:9]=1[CH3:10])[CH3:2].[CH:12]([C:14]1[CH:27]=[CH:26][C:17]([O:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23]([OH:25])=[O:24])=[CH:16][CH:15]=1)=O.[CH2:28]([N:30]1[C:39]2[C:34](=[CH:35][CH:36]=[C:37](O)[CH:38]=2)[C:33](C)=CC1(C)C)[CH3:29].C(C1C=CC(OCC(O)=O)=CC=1)=O>CO>[CH2:1]([NH:3][C:4]1[C:9]([CH3:10])=[CH:8][C:7]2[C:12]([C:14]3[CH:27]=[CH:26][C:17]([O:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23]([OH:25])=[O:24])=[CH:16][CH:15]=3)=[C:36]3[C:37]([O:11][C:6]=2[CH:5]=1)=[CH:38]/[C:39](=[N:30]/[CH2:28][CH3:29])/[C:34]([CH3:33])=[CH:35]3)[CH3:2]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Dye 10 (shown below) was prepared using the procedure described in Example 4 except that 3-(ethylamino)-4-methylphenol and 5-(4-formylphenoxy)pentanoic acid substituted for 1-ethyl-2,2,4-trimethyl-1,2-dihydroquinolin-7-ol and 2-(4-formylphenoxy)acetic acid. Yield: 17%. λabs=524 nm (in methanol), λem=541 nm (in methanol).
Aufarbeitung
- customDye 10 (shown below) was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-f961227f27cc4aaeabe09d2a8a01348e
- Quelldatensatz
- uspto-grants-2016_08
- Patentnummer
- US09416153B2
Verknüpfte Notizen
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