Reaktionsgleichung
[CH3:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[O:9][CH3:10].[CH2:11]([C:13]([CH2:20][CH3:21])([C:17](Cl)=[O:18])[C:14](Cl)=[O:15])[CH3:12].[Cl-].[Al+3].[Cl-].[Cl-]>CCCCCC>[CH2:11]([C:13]1([CH2:20][CH3:21])[C:14](=[O:15])[C:6]2[C:5](=[CH:4][C:3]([O:9][CH3:10])=[C:2]([CH3:1])[C:7]=2[CH3:8])[C:17]1=[O:18])[CH3:12]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
A stirred mixture of 2,3-dimethylanisole (6.8 g., 0.05 mole) and 2,2-diethylmalonyl chloride (10 g., 0.051 mole) in hexane (75ml.) is cooled to 0°C. and treated with aluminum chloride (13.5 g., 0.11 mole) in several portions over a 15 minute period. The reaction is heated at reflux for 2 hours, the hexane is distilled at reduced pressure, the product treated with cold 1N-hydrochloric acid, extracted into ether, washed with water, 5% sodium hydroxide, water then dried over magnesium sulfate. Evaporation of the ether at reduced pressure affords 6.3 g. of 2,2-diethyl-4,5-dimethyl-6-methoxy-indan-1,3-dione which melts at 80°-81°C. after recrystallization from petroleum ether.
Aufarbeitung
- temperatureThe reaction is heated
- temperatureat reflux for 2 hours
- distillationthe hexane is distilled at reduced pressure
- additionthe product treated with cold 1N-hydrochloric acid
- extractionextracted into ether
- washwashed with water, 5% sodium hydroxide, water
- dry with materialthen dried over magnesium sulfate
- customEvaporation of the ether at reduced pressure
- customaffords 6.3 g
- customof 2,2-diethyl-4,5-dimethyl-6-methoxy-indan-1,3-dione which melts at 80°-81°C. after recrystallization from petroleum ether
Quellen und Nachweise
- ORD-Eintrag
- ord-94cc5e6a289f47d2b4a6e9a041479a95
- Quelldatensatz
- uspto-grants-1976_06
- Patentnummer
- US03966966
Verknüpfte Notizen
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