Reaktion #2021944
ord-a443625fe5794a98a310111b4c17b34a
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1TemperaturWhile refluxing the suspension
- 2Temperaturunder reflux for one hour
- 3Sonstigewas elevated to ambient temperature
- 4workup.STIRRINGAfter stirring the mixture at the same temperature as above, the reaction mixture
- 5workup.STIRRINGstirred at ambient temperature for 20 minutes
- 6Extraktionextracted with ethyl acetate
- 7WaschenThe organic layer was washed successively with water and saturated aqueous solution of sodium chloride
- 8Trocknendried over anhydrous magnesium sulfate
- 9workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 10SonstigePurification of the residue by column chromatography [eluent: hexane:ethyl acetate=3:1]
Vorschrift
In an atmosphere of nitrogen, 0.23 g of magnesium powder was suspended in 2 ml of anhydrous ethyl ether. While refluxing the suspension, a solution of 2.00 g of 4-tert-butyl-1-bromobenzene in 10 ml anhydrous ethyl ether was dropwise added. After stirring the resulting mixture under reflux for one hour, a solution of 1.17 g of 1,4-cyclohexandione monoethylene ketal in 10 ml anhydrous tetrahydrofuran was dropwise added at 0-5° C., and the temperature was elevated to ambient temperature. After stirring the mixture at the same temperature as above, the reaction mixture was poured into a mixture of water and acetic acid, stirred at ambient temperature for 20 minutes, and extracted with ethyl acetate. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by column chromatography [eluent: hexane:ethyl acetate=3:1] gave 1.25 of 8-[4-(tert-butyl)phenyl]-1,4-dioxaspiro[4.5]decan-8-ol as a light yellow oily product.