HRID421526

反应详情

EQUATION

反应方程式

HRID 421526 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Into a 300 mL three-neck flask was put 4.9 g (17 mmol) of 2-bromo-9,10-anthraquinone, the atmosphere in the flask was substituted with nitrogen, and 100 mL of tetrahydrofuran (THF) was added thereto and dissolved well. Then, 18 mL (37 mmol) of phenyllithium was dropped into this solution, followed by stirring at room temperature for about 12 hours. After the reaction, the solution was washed with water, and an aqueous layer was extracted with ethyl acetate. The extract was combined with an organic layer to be dried with magnesium sulfate. After the drying, the mixture was suction filtered, and the filtrate was concentrated to give 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol, which was the object of the synthesis (about 7.6 g).

WORKUP

后处理

  1. customInto a 300 mL three-neck flask was put
  2. additionwas added
  3. dissolutiondissolved well
  4. customAfter the reaction
  5. washthe solution was washed with water
  6. extractionan aqueous layer was extracted with ethyl acetate
  7. dry with materialto be dried with magnesium sulfate
  8. filtrationfiltered
  9. concentrationthe filtrate was concentrated