Reacción #7293
ord-055226509f2c42309f67211cf933f618
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroequipped with a stirrer
- 2Temperaturathe reaction mixture was cooled down to room temperature
- 3Filtraciónwas filtered off
- 4Otrothe solvent was removed under a reduced pressure
- 5workup.DISSOLUTIONThe residue was dissolved in chloroform
- 6Lavadoresultant was washed with water several times
- 7Secadodried with anhydrous magnesium sulfate, which
- 8Filtraciónwas then filtered off
- 9OtroThe solvent was removed
- 10Otrothe residue was recrystallized from ethyl acetate/hexane mixture
- 11Otroto obtain pale yellow crystal, which
- 12Otrowas sufficiently dried in a vacuum oven at 40° C.
Procedimiento
100 g (0.338 mol) of 1,4-dibromo-2,5-dimethoxybenzene, 7.12 g (0.01 mol) of bistriphenylphospine palladium dichloride and 1.93 g (0.01 mol) of copper iodide were put into a 1 litter 3-neck round-bottom flask equipped with a stirrer, a thermometer and a reflux condenser under an argon atmosphere, and dissolved in 600 ml of diisopropylamine. 99 g (1 mol) of trimethylsilylacetylene was then slowly added dropwise at room temperature, and stirred at 80° C. for 12 hours. When the reaction was completed, the reaction mixture was cooled down to room temperature, generated salt was filtered off, and then the solvent was removed under a reduced pressure. The residue was dissolved in chloroform, and resultant was washed with water several times and then dried with anhydrous magnesium sulfate, which was then filtered off. The solvent was removed, and the residue was recrystallized from ethyl acetate/hexane mixture to obtain pale yellow crystal, which was sufficiently dried in a vacuum oven at 40° C. to give 82.5 g (yield: 73%) of the desired product, and its melting point was 164° C.–165° C.