HCID 54296870, Verbindung → 1,4-Dihydro-2,6-dimethyl-3,5-dinitro-4-(3-nitrophenyl)pyridine
Reaktionsgleichung
[N+:1]([C:4]([C:15](=O)[CH3:16])=[CH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)([O-:3])=[O:2].[NH2:18][C:19]([CH3:24])=[CH:20][N+:21]([O-:23])=[O:22]>C(O)C>[CH3:16][C:15]1[NH:18][C:19]([CH3:24])=[C:20]([N+:21]([O-:23])=[O:22])[CH:5]([C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=2)[C:4]=1[N+:1]([O-:3])=[O:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
23.6 g (0.1 mol) of 2-nitro-1-(3nitrophenyl)-but-1-ene-3-one and 10.2 g (0.1 mol) of 2-amino-1-nitro-prop-1-ene in 150 ml of ethanol were heated under reflux for 12 hours. After the mixture had cooled, the solvent was distilled off in vacuo, and the oily residue was taken up in chloroform, and was chromatographed on a silica gel column, using chloroform with the addition of methanol. The product formed yellow crystals of melting point 237°-240° C. (decomposition) in isopropanol.