Reaktionsgleichung
[CH3:1][NH2:2].[N+:3]([C:6]1[CH:17]=[CH:16][C:9]2[CH2:10][CH2:11][CH:12]=[CH:13][C:14](=[O:15])[C:8]=2[CH:7]=1)([O-:5])=[O:4]>C1C=CC=CC=1.C(O)C>[N+:3]([C:6]1[CH:17]=[CH:16][C:9]2[CH2:10][CH2:11][CH:12]([NH:2][CH3:1])[CH2:13][C:14](=[O:15])[C:8]=2[CH:7]=1)([O-:5])=[O:4]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 101.5 g of extemporaneously prepared monomethylamine in 700 ml of benzene was added at 20° C. with stirring to a mixture of 101.6 g of the product of Step B in 1 liter of ethanol and the mixture was stirred for 2 1/2 hours at room temperature and was allowed to stand for 12 hours. The mixture was evaporated to dryness under reduced pressure to obtain 125 g of 3-nitro-7-methylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene-5-one in the form of a brown oil.
Aufarbeitung
- waitto stand for 12 hours
- customThe mixture was evaporated to dryness under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-f667e65404f64712858a672b6d42047c
- Quelldatensatz
- uspto-grants-1979_05
- Patentnummer
- US04154852
Verknüpfte Notizen
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