Reaktionsgleichung
[N+:1]([C:4]1[CH:17]=[CH:16][CH:15]=[C:14]2[C:5]=1[C:6](=[O:19])[CH:7]1[CH:12]([C:13]2=[O:18])[CH2:11][CH:10]=[CH:9][CH2:8]1)([O-])=[O:2].C(N)CCC>C1(C)C=CC=CC=1>[OH:2][NH:1][C:4]1[C:5]2[C:6](=[O:19])[C:7]3[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=3)[C:13](=[O:18])[C:14]=2[CH:15]=[CH:16][CH:17]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
A mixture of 5.0 parts of 5-nitro-1,4,4a,9a-tetrahydroanthraquinone with 80 parts of toluene and 1.0 part of n-butylamine was stirred at 70°C for 2 hours. The mixture was then distilled under a reduced pressure of 100 mm Hg to remove toluene, washed with 50 parts of methanol and dried under reduced pressure to obtain 4.4 parts of 1-hydroxylaminoanthraquinone.
Aufarbeitung
- distillationThe mixture was then distilled under a reduced pressure of 100 mm Hg
- customto remove toluene
- washwashed with 50 parts of methanol
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-b3584de3cd3b4e89ac040e3cef6b4bc3
- Quelldatensatz
- uspto-grants-1976_06
- Patentnummer
- US03966775
Verknüpfte Notizen
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