Reaktionsgleichung
[CH3:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:12].[OH-].[K+].[CH2:15](Br)[CH:16]=[CH:17][CH3:18]>CO>[CH3:1][C:2]1[CH:10]=[CH:9][C:8]([O:11][CH2:15][CH:16]=[CH:17][CH3:18])=[C:7]2[C:3]=1[CH2:4][CH2:5][C:6]2=[O:12]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Into a solution of 10 g of 4-methyl-7-hydroxy-1-indanone and 5.3 g of potassium hydroxide in 200 ml of methanol was added 8.2 ml of crotyl bromide, and the mixture was refluxed by heating for 4 hours. The insoluble matters in the reaction mixture were removed by filtration, then the solvent was removed by evaporation. The residue obtained was extracted with chloroform-water, and the chloroform layer was washed with a diluted sodium hydroxide aqueous solution, then washed with water, dried with anhydrous magnesium sulfate, and the solvent was removed by evaporation. The residue obtained was purified by means of a silica gel column chromatography (eluent: n-hexane: dichloromethane=1:1) to obtain 8.72 g of 4-methyl-7-crotyloxy-1-indanone.
Aufarbeitung
- temperaturethe mixture was refluxed
- temperatureby heating for 4 hours
- customThe insoluble matters in the reaction mixture were removed by filtration
- customthe solvent was removed by evaporation
- customThe residue obtained
- extractionwas extracted with chloroform-water
- washthe chloroform layer was washed with a diluted sodium hydroxide aqueous solution
- washwashed with water
- dry with materialdried with anhydrous magnesium sulfate
- customthe solvent was removed by evaporation
- customThe residue obtained
- customwas purified by means of a silica gel column chromatography (eluent: n-hexane: dichloromethane=1:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-c5e1de5bb72f45a59afd3faaff265cc2
- Quelldatensatz
- uspto-grants-1988_12
- Patentnummer
- US04792628
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