Reaktionsgleichung
O[C:2]1([CH3:11])[CH:6]([CH2:7][CH:8]=[CH2:9])[C:5](=[O:10])[CH:4]=[CH:3]1.[Cl-].[Na+].[OH2:14]>>[CH2:7]([C:6]1[C:5](=[O:10])[CH2:4][CH:3]([OH:14])[C:2]=1[CH3:11])[CH:8]=[CH2:9]Komponenten
4
Versuchsvorschrift
In an autoclave, 4-hydroxy-4-methyl-5-allyl-2-cyclopentenone (20 g) and water (400 ml) were charged, and the resultant mixture was stirred at 180° C. for 6 hours in a nitrogen atmosphere. After cooling, sodium chloride (50 g) was added to the reaction mixture, and the resulting mixture was extracted with methyl isobutyl ketone. The extract was concentrated under reduced pressure to give 2-allyl-3-methyl-4-hydroxy-2-cyclopentenone (19 g). Yield, 95%. M.P. 130°-132° C./1.2 mmHg.
Aufarbeitung
- temperatureAfter cooling
- extractionthe resulting mixture was extracted with methyl isobutyl ketone
- concentrationThe extract was concentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-8371605ffe1349dc8bb6c0fe1adc2020
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04347386
Verknüpfte Notizen
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