Reaktionsgleichung
[CH3:1][C:2]([N:6]([CH3:8])[CH3:7])([CH2:4][OH:5])[CH3:3].[C:9](O)(=[O:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]>C1(C)C=CC=CC=1>[C:9]([O:5][CH2:4][C:2]([N:6]([CH3:8])[CH3:7])([CH3:3])[CH3:1])(=[O:17])[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
DMAMP 118 g (1 mole) and commercial grade caprylic acid 131 g (1 mole) were dissolved in 35 ml of toluene. The mixture was heated under reflux at about 140°-165° until 20 ml distillate was recovered and no more was being collected. The pressure was then reduced to 10mm and distillation was continued to about 130° C to strip off toluene and water. The pressure was then reduced to about 1 mm and the main product fraction was recovered at a liquid temperature of about 106°-109°. There was obtained 2-dimethylamino-2-methyl-1-propyl caprylate, neutral equivalent 247.9 compared with theoretical 244.
Aufarbeitung
- temperatureThe mixture was heated
- temperatureunder reflux at about 140°-165° until 20 ml distillate
- customwas recovered
- customno more was being collected
- distillationThe pressure was then reduced to 10mm and distillation
- customwas continued to about 130° C
- customthe main product fraction was recovered at a liquid temperature of about 106°-109°
Quellen und Nachweise
- ORD-Eintrag
- ord-e4a6d84bc127406c9fda6e0c26d748d4
- Quelldatensatz
- uspto-grants-1977_05
- Patentnummer
- US04022909
Verknüpfte Notizen
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