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
1.00 g of N-ethyl-3-bromocarbazole was dissolved in 3.2 ml of dehydrated ether in a Schrenck tube which was flame-dried and argon gas-replaced. This solution was cooled to −78° C., and 2.4 ml of n-butyl lithium (2.64M hexane solution) was added dropwise. After raising the temperature to 0° C., and stirring for 1 hour, it was cooled again to −78° C., an ether solution of magnesium bromide prepared from magnesium 0.4 g and 1,2-dibromoethane 0.8 g was added dropwise. After raising the temperature to room temperature and stirring for 12 hours, this reaction solution was added dropwise into a solution which was prepared by suspending lithium bromide 0.28 g, 3-trifluoromethanesulfoxybromo benzene 0.82 g, and dichloro[1,3-bis(diphenylphosphino)propane]palladium(II) 0.09 g in dehydrated diethylether 2 ml, and cooled at 0° C. After stirring for 7 hours, 20 ml water was added dropwise and partitioned. The aqueous phase was extracted twice with 40 ml toluene, and the combined aqueous phase was washed with water and saturated NaCl aqueous solution, then concentrated, and 1.61 g of crude product was obtained. It was purified with silica gel column chromatography (eluent, hexane:ethyl-acetate=25:1), 0.33 g of N-ethyl-3-(3-bromophenyl)carbazole was obtained.
WORKUP
后处理
- customwas flame-dried
- addition2.4 ml of n-butyl lithium (2.64M hexane solution) was added dropwise
- temperatureAfter raising the temperature to 0° C.
- temperatureit was cooled again to −78° C.
- customan ether solution of magnesium bromide prepared from magnesium 0.4 g and 1,2-dibromoethane 0.8 g
- additionwas added dropwise
- temperatureAfter raising the temperature to room temperature
- stirringstirring for 12 hours
- additionthis reaction solution was added dropwise into a solution which
- customwas prepared
- temperaturecooled at 0° C
- stirringAfter stirring for 7 hours
- custompartitioned
- extractionThe aqueous phase was extracted twice with 40 ml toluene
- washthe combined aqueous phase was washed with water and saturated NaCl aqueous solution
- concentrationconcentrated
- custom1.61 g of crude product was obtained
- customIt was purified with silica gel column chromatography (eluent, hexane:ethyl-acetate=25:1)