Reaktionsgleichung
[CH2:1]([CH2:6][C:7]([CH:9]=[C:10](C)C)=[O:8])[CH:2]=[C:3](C)[CH3:4].C(N)CN.[OH-].[Na+]>>[CH3:10][CH2:9][C:7](=[O:8])[CH:6]=[CH:1][CH2:2][CH2:3][CH3:4]Komponenten
4
Versuchsvorschrift
A 500 ml flask was charged with 100.0 g of prenyl mesityl oxide (13% nonconjugated 79.7% conjugated isomer), 0.56 mole, 40.6 g ethylene diamine, and 0.5 g NaOH. This was then flushed thoroughly with nitrogen. The mixture was heated at between 95° and 105° C. and agitated for approximately four hours under a slight nitrogen pressure. Analysis by gas liquid chromatography indicated that 31.9% prenyl mesityl oxide remained unchanged after this time. Steam distillation of the pot mixture gave a true yield of 95.8% of methyl heptenone based on the prenyl mesityl oxide reacted, after the recovery of unreacted prenyl mesityl oxide.
Aufarbeitung
- customThis was then flushed thoroughly with nitrogen
- temperatureThe mixture was heated at between 95° and 105° C.
- distillationSteam distillation of the pot mixture
Quellen und Nachweise
- ORD-Eintrag
- ord-b6eefbb5675d4d5fa52ef55c81be5471
- Quelldatensatz
- uspto-grants-1979_05
- Patentnummer
- US04153633
Verknüpfte Notizen
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