Isobutyraldehyde → 3-Ethyl-2-(propan-2-yl)-1,3-oxazolidine
Reaktionsgleichung
[CH:1](=[O:5])[CH:2]([CH3:4])[CH3:3].[CH2:6]([NH:8][CH2:9][CH2:10]O)[CH3:7]>C1C=CC=CC=1>[CH:2]([CH:1]1[N:8]([CH2:9][CH3:10])[CH2:6][CH2:7][O:5]1)([CH3:4])[CH3:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Iso-butyraldehyde (11.1 g; 0.15 moles) was added slowly over a period of 1 hour to N-ethyl-2-hydroxyethylamine (13.3 g; 0.15 moles) at a temperature of 25°-30° C. Benzene (100 ml) was then added, and the resulting solution was heated to reflux. Continuous azeotropic distillation removed 2.8 ml of water. The benzene was then removed by vacuum distillation to give the desired 2-isopropyl-3-ethyl-1,3-oxazolidine as a yellow liquid.
Aufarbeitung
- temperaturethe resulting solution was heated to reflux
- distillationContinuous azeotropic distillation
- customremoved 2.8 ml of water
- customThe benzene was then removed by vacuum distillation
Quellen und Nachweise
- ORD-Eintrag
- ord-9b4f380f3806411aab25c8692a8df7e9
- Quelldatensatz
- uspto-grants-1982_01
- Patentnummer
- US04311827
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