Ethyl formate → N-Cyclohexyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)formamide
Reaktionsgleichung
[CH:1]1([NH:7][CH:8]2[CH2:13][C:12]([CH3:15])([CH3:14])[NH:11][C:10]([CH3:17])([CH3:16])[CH2:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:18](OCC)=[O:19]>CCCCO.CCCCO.CCCCO.CCCCO.[Ti]>[CH:1]1([N:7]([CH:8]2[CH2:13][C:12]([CH3:15])([CH3:14])[NH:11][C:10]([CH3:17])([CH3:16])[CH2:9]2)[CH:18]=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
80 g of 4-(N-cyclohexylamino)-2,2,6,6-tetramethylpiperidine and 32 g of tetrabutyl orthotitanate in 175 ml of ethyl formate were refluxed for 11 hours. Fractional distillation gave a fraction of boiling point 143°-144° C. under 0.4 mmHg. After solidification, this fraction was recrystallized from n-hexane. 4-(N-cyclohexyl-N-formylamino)-2,2,6,6-tetramethylpiperidine was isolated as a colorless solid of melting point 105° C.