反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -78 °C
PROCEDURE
实验过程
Under a stream of argon, 2.1 ml of a hexane solution containing 3.3 mmol of butyl lithium was slowly added to 70 ml of tetrahydrofuran cooled to −78° C. in which 1.62 g of 2,4-bis(4-biphenylyl)-6-(4-bromophenyl)-1,3,5-triazine obtained in Reference Example 3 had been dissolved. After stirring at −78° C. for 15 minutes, 0.91 g of dichloro(tetramethylethylenediamine)zinc(II) was added thereto and stirred at −78° C. for 10 minutes and then at room temperature for 2 hours. A 20 ml portion of tetrahydrofuran prepared by dissolving 0.85 g of 6-bromo-2,2′-bipyridyl and 0.14 g of tetrakis(triphenylphosphine)palladium(0) therein was added to this solution and stirred under heating reflux for 4 hours. The reaction solution was concentrated under a reduced pressure and the thus obtained solid was recrystallized from dichloromethane-methanol. The thus obtained crude product was washed with chloroform to obtain a white solid of the intended 6-{4-[4,6-bis(4-biphenylyl)-1,3,5-triazin-2-yl]phenyl}-2,2′-bipyridyl (1.24 g, yield 67%).
WORKUP
后处理
- customobtained in Reference Example 3
- dissolutionhad been dissolved
- stirringstirred at −78° C. for 10 minutes
- waitat room temperature for 2 hours
- additiontherein was added to this solution
- stirringstirred
- temperatureunder heating
- temperaturereflux for 4 hours
- concentrationThe reaction solution was concentrated under a reduced pressure
- customthe thus obtained solid was recrystallized from dichloromethane-methanol
- customThe thus obtained crude product
- washwas washed with chloroform