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
PROCEDURE
实验过程
To a 2 liter Schlenk flask was added (2-iodo-3,4,5-trimethoxyphenyl) diphenylphosphine oxide 21 (30 g, 61 mmol), phenylboronic acid (11.1 g, 91 mmol), and degassed THF (800 ml). A solution of degassed saturated K2CO3 (400 ml) was added afterwards. The whole mixture was degassed with nitrogen for an additional 10 min. Then, Pd(PPh3)4 (1.22 mmol, 1.4 g) was added in the solution through one portion. The mixture was stirred at reflux under nitrogen for 24 hrs. In situ 31PNMR showed that the reaction was complete. The reaction mixture was concentrated under reduced pressure to remove THF and 400 ml of CH2Cl2 was then added. The CH2Cl2 layer was washed with water (200 ml) and brine (200 ml), dried over Na2SO4, and evaporated. The solid residue was recrystallized from EtOAc (100 ml) to give off-white product 22 (23 g). The mother liquid was passed though a silica gel column to give another 4 g of product 22. The total yield was 98%.
WORKUP
后处理
- customdegassed THF (800 ml)
- additionA solution of degassed saturated K2CO3 (400 ml) was added afterwards
- customThe whole mixture was degassed with nitrogen for an additional 10 min
- temperatureat reflux under nitrogen for 24 hrs
- concentrationThe reaction mixture was concentrated under reduced pressure
- customto remove THF and 400 ml of CH2Cl2
- additionwas then added
- washThe CH2Cl2 layer was washed with water (200 ml) and brine (200 ml)
- dry with materialdried over Na2SO4
- customevaporated
- customThe solid residue was recrystallized from EtOAc (100 ml)