Reaktionsgleichung
[OH-].[K+].[Cl:3][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH2:6][CH2:7][C:8]2=O.[CH3:14]I.O.CN(C)[CH:19]=[O:20]>>[CH3:14][C:7]1([CH3:8])[CH2:6][C:5]2[C:9](=[CH:10][CH:11]=[CH:12][C:4]=2[Cl:3])[C:19]1=[O:20]Komponenten
Versuchsvorschrift
22.4 g of pulverized potassium hydroxide and 0.1 g of 18-dibenzocrown-6 are added portionwise to a solution of 25 g of 4-chloroindanone and 56.7 g of methyl iodide in 120 ml of dimethylformamide in such a manner that the temperature is kept below +70° C. When the exothermic reaction is over, 5.6 g of methyl iodide are added and the mixture is agitated for another 0.5 hours. 200 ml of cold water are added and the mixture is extracted with diethyl ether. The organic phase is dried, with sodium sulfate and concentrated to dryness, affording 27.4 g of crude 2,2-dimethyl-4-chloro-indanone. This crude product is directly subjected to the Leuckart-Wallach amine preparation as described in "Organic Reactions vol. 5, page 301ff, John Wiley & Sons, New York 1949", yielding pure 1-amino-4-chloro-2,2-dimethyl-indane.
Aufarbeitung
- customis kept below +70° C
- customWhen the exothermic reaction
- additionare added
- extractionthe mixture is extracted with diethyl ether
- dry with materialThe organic phase is dried, with sodium sulfate
- concentrationconcentrated to dryness
Quellen und Nachweise
- ORD-Eintrag
- ord-65d806fc62d34034938ca2f29c783c94
- Quelldatensatz
- uspto-grants-1993_09
- Patentnummer
- US05246915
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