N-4-Piperidylbenzamide → 2-(4-Benzamidopiperidino)ethylhydroxymethyl ketone
Reaktionsgleichung
[C:1]([NH:9][CH:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH:16][CH2:17][C:18]([CH:20]=[CH2:21])=[O:19]>C(O)C>[C:1]([NH:9][CH:10]1[CH2:15][CH2:14][N:13]([CH2:21][CH2:20][CH:18]([C:17]([CH:1]([OH:8])[CH2:2][CH2:3][N:13]2[CH2:14][CH2:15][CH:10]([NH:9][C:1](=[O:8])[C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH2:11][CH2:12]2)=[O:16])[OH:19])[CH2:12][CH2:11]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-Benzamidopiperidine (2.4 g.) in ethanol (15 ml.) was added to hydroxymethylvinyl ketone (2.0 g.). An exothermic reaction occured and crystallisation occurred on cooling to give 2-(4-benzamidopiperidino)ethylhydroxymethyl ketone, m.p. 154°-155° C. (Found: C, 65.9; H, 7.7; N, 9.5; C16H22N2O3 requires C, 66.2; H, 7.6; N, 9.65%).