Reaktion #508022
ord-402fffcd5878420586152774bbd5ed6c
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturunder reflux
- 2Temperaturby heating
- 3EinengenThe reaction mixture was concentrated under reduced pressure
- 4workup.DISSOLUTIONthe residue was dissolved in hexane
- 5FiltrationThe solution was filtered through silica gel
- 6Einengenthe filtrate was concentrated under reduced pressure
- 7workup.DISSOLUTIONThe resulting residue was dissolved in diethyl ether
- 8workup.ADDITIONthe solution was added with cesium fluoride (1.01 g)
- 9workup.STIRRINGthe mixture was stirred at room temperature for 30 minutes
- 10workup.ADDITIONThe reaction mixture was added with a mixed solvent of hexane
- 11Filtrationethyl acetate=10:1, and the mixture was filtered
- 12EinengenThe filtrate was concentrated under reduced pressure
- 13Sonstigethe resulting residue was purified by silica gel column chromatography (hexane alone)
Vorschrift
1,3-Dibromobenzene (1.0 g) was dissolved in toluene (20 ml), the solution was added with tri-n-butyl-(2-furyl)tin 1.59 g) and tetrakistriphenylphosphine palladium (0.25 g), and the mixture was stirred for 30 minutes under reflux by heating. The reaction mixture was concentrated under reduced pressure, and then the residue was dissolved in hexane. The solution was filtered through silica gel, and the filtrate was concentrated under reduced pressure. The resulting residue was dissolved in diethyl ether, the solution was added with cesium fluoride (1.01 g), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was added with a mixed solvent of hexane:ethyl acetate=10:1, and the mixture was filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane alone) to obtain the title compound (0.59 g).