3-amino-N-ethylpiperidine → HCID 70401954, Verbindung

HRID 34568

Reaktionsgleichung

Reaktionsgleichung von HRID 34568
[CH3:1][C:2]([CH2:7][CH2:8][CH:9]=[C:10]([CH3:22])[CH2:11][CH2:12][CH:13]=[C:14]([CH3:21])[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19])=[CH:3][C:4]([OH:6])=O.[NH2:23][CH:24]1[CH2:29][CH2:28][CH2:27][N:26]([CH2:30][CH3:31])[CH2:25]1>>[CH3:1][C:2]([CH2:7][CH2:8][CH:9]=[C:10]([CH3:22])[CH2:11][CH2:12][CH:13]=[C:14]([CH3:21])[CH2:15][CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19])=[CH:3][C:4]([NH:23][CH:24]1[CH2:29][CH2:28][CH2:27][N:26]([CH2:30][CH3:31])[CH2:25]1)=[O:6]

Komponenten

3

Edukt 2

HCID 980943-amino-N-ethylpiperidineHCID 1285703,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acid

Produkt 1

HCID 70401954HCID 70401954, VerbindungAusbeute 90 %

Versuchsvorschrift

The procedure of Example 9 was repeated except that 6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid and 3.8 g of 3-amino-1-ethylpiperidine were used as starting materials. 7.4 g (yield 90%) of the title compound was obtained as a pale yellow oil.

Quellen und Nachweise

ORD-Eintrag
ord-f701844bc00c40f397e9dffa89ea098d
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04762829

Verknüpfte Notizen

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