HRID1429338

反应详情

EQUATION

反应方程式

HRID 1429338 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-60 °C

PROCEDURE

实验过程

In argon atmosphere, a liquid mixture of 7.47 g (20.0 mmol) of 2-(6-bromonaphthalene-2-yl)dibenzofuran and 75 ml of dry THF was cooled to −60° C., and 15.5 ml (24.0 mmol) of a 1.55 M hexane solution of n-butyllithium was added dropwise under stirring. Further, the reaction mixture was stirred at −70° C. for 2 h. The reaction solution was cooled again to −70° C., and 11.29 g (60.0 mol) of triisopropyl borate was added dropwise. The reaction mixture was heated up to room temperature, stirred for one hour, and left standing overnight. The reaction mixture was cooled on an ice bath, added with a 6 N hydrochloric acid, and stirred at room temperature for one hour. After adding dichloromethane, the reaction mixture was allowed to separate into liquid phases, and the organic phase was washed with water and dried over sodium sulfate. The solvent was removed by distillation under reduced pressure, and the residue was purified by silica gel chromatography to obtain 4.20 g (yield: 62%) of 6-(dibenzofuran-2-yl)naphthalene-2-ylboronic acid.

WORKUP

后处理

  1. stirringFurther, the reaction mixture was stirred at −70° C. for 2 h
  2. temperatureThe reaction solution was cooled again to −70° C.
  3. temperatureThe reaction mixture was heated up to room temperature
  4. stirringstirred for one hour
  5. waitleft
  6. temperatureThe reaction mixture was cooled on an ice bath
  7. stirringstirred at room temperature for one hour
  8. customto separate into liquid phases
  9. washthe organic phase was washed with water
  10. dry with materialdried over sodium sulfate
  11. customThe solvent was removed by distillation under reduced pressure
  12. customthe residue was purified by silica gel chromatography