HRID2173745

反应详情

EQUATION

反应方程式

HRID 2173745 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

First, 3.0 g of 2,7-dibromonaphthalene was placed into a 500-mL three-neck flask, and the air in the flask was replaced with nitrogen. To this compound was added 150 mL of tetrahydrofuran (THF), and this solution was stirred at −78° C. for 20 minutes. Then, 6.4 mL of a 1.7M hexane solution of n-butyllithium (n-BuLi) was dripped into this mixture solution, followed by stirring at −78° C. for 2 hours. After the predetermined time had elapsed, 2.4 mL of trimethyl borate was added to the mixture and this solution was stirred for 18 hours while the temperature was raised to room temperature. After the predetermined time had elapsed, 60 mL of 1.0M hydrochloric acid was poured into this solution, and the mixture was stirred for 1 hour. Then, this mixture solution was separated into an organic layer and an aqueous layer. Organic substances were extracted with ethyl acetate from the obtained aqueous layer. The solution of the extract was combined with the organic layer that had been first obtained, and the mixture was washed with saturated brine and dried by addition of anhydrous magnesium sulfate to the organic layer. Then, the filtrate obtained by gravity filtration was concentrated to give a white solid. The obtained white solid was washed with a mixed solvent of hexane and toluene, whereby 7-bromonaphthalene-2-boronic acid was obtained (as a white powder in 75% yield). The synthesis scheme of Step 1 is illustrated in the following (a-5).

WORKUP

后处理

  1. stirringby stirring at −78° C. for 2 hours
  2. stirringthis solution was stirred for 18 hours while the temperature
  3. temperaturewas raised to room temperature
  4. stirringthe mixture was stirred for 1 hour
  5. customThen, this mixture solution was separated into an organic layer
  6. extractionOrganic substances were extracted with ethyl acetate from the obtained aqueous layer
  7. customhad been first obtained
  8. washthe mixture was washed with saturated brine
  9. dry with materialdried by addition of anhydrous magnesium sulfate to the organic layer
  10. customThen, the filtrate obtained by gravity filtration
  11. concentrationwas concentrated
  12. customto give a white solid
  13. washThe obtained white solid was washed with a mixed solvent of hexane and toluene