HRID1184047

反应详情

EQUATION

反应方程式

HRID 1184047 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4.9 g (17 mmol) of 2-bromo-9,10-anthraquinone was put into a 300 mL three-neck flask. The atmosphere in the flask was substituted with nitrogen. 100 mL of tetrahydrofuran (THF) was added and dissolved well. After that, 18 mL (37 mmol) of phenyl lithium was dripped into the solution, and the mixture was stirred at room temperature for about 12 hours. After the reaction, the solution was washed with water. Then, the aqueous layer was extracted with ethyl acetate. The extracted solution and an organic layer were mixed to be dried with magnesium sulfate. After the drying, this mixture was suction-filtrated and the filtrate was concentrated, so that 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol (about 7.6 g), which was an object, was obtained.

WORKUP

后处理

  1. dissolutiondissolved well
  2. customAfter the reaction
  3. washthe solution was washed with water
  4. extractionThen, the aqueous layer was extracted with ethyl acetate
  5. additionThe extracted solution and an organic layer were mixed
  6. dry with materialto be dried with magnesium sulfate
  7. filtrationAfter the drying, this mixture was suction-filtrated
  8. concentrationthe filtrate was concentrated, so that 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol (about 7.6 g), which
  9. customwas obtained