Reaktionsgleichung
C(O)(CC)C.[N+:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N:15]=[N:16][C:17]1[CH:22]=[C:21]([C:23]([CH3:26])([CH3:25])[CH3:24])[CH:20]=[CH:19][C:18]=1[OH:27])([O-:8])=O.[N+](C1C=CC=CC=1N=NC1C=C(C(C)(C)C)[CH:42]=[C:41]([C:49](C)(C)C)[C:40]=1O)([O-])=O>C(O)CCCCCCC>[OH:27][C:18]1[C:19]([C:41]([CH3:49])([CH3:42])[CH3:40])=[CH:20][C:21]([C:23]([CH3:26])([CH3:24])[CH3:25])=[CH:22][C:17]=1[N:16]1[N+:6]([O-:8])=[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]2=[N:15]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The same procedure as in Example 7 was repeated, except that secondary butanol 80 g was replaced by n-octanol 50 g, and that 2-nitro-2'-hydroxy-5'-t-butylazobenzene 19.9 g was replaced by 2-nitro-2'-hydroxy-3',5'-di-t-butylazobenzene 23.7 g, thus producing 18.7 g of 2-(2-hydroxy-3,5-di-t-butylphenyl)benzotriazole-N-oxide having a melting point of 168° to 171° C. at the yield of 83.0%.
Quellen und Nachweise
- ORD-Eintrag
- ord-c7f3c064070f403d971d820c933b16c7
- Quelldatensatz
- uspto-grants-1990_07
- Patentnummer
- US04943637
Verknüpfte Notizen
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