Reaktion #7292
ord-69e50f4a0a4148ad88f1efb062fdfe32
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeequipped with a stirrer
- 2Temperaturthe reaction mixture was cooled down to room temperature
- 3Filtrationwas filtered off
- 4SonstigeThe solvent was removed under a reduced pressure
- 5Extraktionthe residue was extracted with methylene chloride
- 6WaschenOrganic layer was washed with water several times
- 7Trocknendried with anhydrous magnesium sulfate
- 8Sonstigethe solvent was removed
- 9Sonstigeto obtain yellow solid
- 10SonstigeThis solid was recrystallized from ethyl acetate
- 11Sonstigeto obtain yellow crystal, which
- 12Sonstigewas sufficiently dried in a vacuum oven at 40° C.
Vorschrift
50 g (160 mmol) of 1,4-dibromo-2,5-dimethoxy benzene, 3.6 g (0.005 mol) of bistriphenylphosphine palladium dichloride and 0.97 g (0.005 mol) of copper iodide were put into a 1 litter 3-neck flask equipped with a stirrer, a thermometer and a reflux condenser under an argon atmosphere, and dissolved in 500 ml of piperidine. 43 g (0.422 mol) of phenylacetylene was then slowly added dropwise at room temperature. The reaction temperature was slowly raised to 80° C. and then the reaction mixture was stirred at the same temperature for 12 hours. When the reaction was completed, the reaction mixture was cooled down to room temperature, and then generated salt was filtered off. The solvent was removed under a reduced pressure, and then the residue was extracted with methylene chloride. Organic layer was washed with water several times and dried with anhydrous magnesium sulfate, and then the solvent was removed to obtain yellow solid. This solid was recrystallized from ethyl acetate to obtain yellow crystal, which was sufficiently dried in a vacuum oven at 40° C. to give 41 g (yield: 72%) of the desired product, and its melting point was 172° C.–174° C.