HRID420020

反应详情

EQUATION

反应方程式

HRID 420020 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

In a 500 mL three-neck flask was put 21.8 g (67.5 mmol) of 9-(4-bromophenyl)-9H-carbazole. The atmosphere in the flask was replaced with nitrogen. To the mixture was added 200 mL of tetrahydrofuran (THF). The temperature of this solution was set to −78° C., and then 48.9 mL (74.3 mmol) of n-butyllithium (a 1.52 mol/L hexane solution) was dripped to the solution. The mixture was stirred at the same temperature for 2 hours. After that, 17.4 mL (155 mmol) of trimethyl borate was added to the mixture, followed by stirring for 1 hour at the same temperature. Then, the mixture was stirred for 24 hours while the temperature thereof is returned to room temperature. After that, 200 mL of 1.0 mol/L hydrochloric acid was added to this solution, followed by stirring for 1 hour at room temperature. The organic layer of the mixture was washed with water, and the aqueous layer was extracted with ethyl acetate. The extract and the organic layer were combined, washed with saturated brine, and then dried with magnesium sulfate. After that, this mixture was suction filtered. The resulting filtrate was concentrated to give a residue. This residue was recrystallized with a mixed solvent of chloroform and hexane to give 4-(9H-carbazol-9-yl)phenylboronic acid which was the desired substance as 13 g of a white powdered solid in a yield of 66%.

WORKUP

后处理

  1. customIn a 500 mL three-neck flask was put
  2. customwas set to −78° C.
  3. stirringby stirring for 1 hour at the same temperature
  4. stirringThen, the mixture was stirred for 24 hours while the temperature
  5. customthereof is returned to room temperature
  6. stirringby stirring for 1 hour at room temperature
  7. washThe organic layer of the mixture was washed with water
  8. extractionthe aqueous layer was extracted with ethyl acetate
  9. extractionThe extract
  10. washwashed with saturated brine
  11. dry with materialdried with magnesium sulfate
  12. filtrationfiltered
  13. concentrationThe resulting filtrate was concentrated
  14. customto give a residue
  15. customThis residue was recrystallized with a mixed solvent of chloroform and hexane