Benzene → HCID 178420620, Verbindung

Reaktionsgleichung

[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[O:10][CH3:11].C([CH:15](C([NH:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24]C=1)=O)[C:16]([OH:18])=[O:17])(O)=O.[NH:28]1[CH2:33][CH2:32][CH2:31][CH2:30][CH2:29]1.[OH2:34].[CH:35]1[CH:40]=CC=CC=1>>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[CH:40][C:35]([NH:28][C:33]2[C:15](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:16]([O-:18])=[O:17])=[O:34])=[CH:4][C:3]=1[O:10][CH3:11].[NH2+:21]1[CH2:22][CH2:27][CH2:26][CH2:25][CH2:24]1

Komponenten

Edukt 5

HCID 20222317HCID 20222317, Verbindung

Produkt 1

HCID 178420620HCID 178420620, Verbindung

Versuchsvorschrift

A solution of 2.54 g of 4-hydroxy-3-methoxybenzaldehyde, 3.8 g of 2-carboxymalonanilic acid, and 4.29 g of piperidine in 17 ml of benzene is heated for 3 hours under reflux with removal of water of reaction. After completion of the reaction, the reaction mixture is cooled and the precipitated crystals are collected by filtration and dried to obtain 6.34 g of piperidinium N-(4-hydroxy-3-methoxycinnamoyl)anthranilate, mp. 188°-189° C. The compound structure is confirmed by elemental analysis, and by IR and NMR spectroscopy.