HRID36440

反应详情

EQUATION

反应方程式

HRID 36440 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

In 20 ml of methylene chloride were dissolved 0.62 g of m-anisidine and 5 ml of triethylamine. To this solution was added dropwise under ice cooling 20 ml of methylene chloride containing 2.64 g of 2-[bis(4-acetoxyphenyl)methyl]benzoyl chloride as obtained in Reference Example 2. After stirring for 30 minutes, water was added thereto. The organic layer was separated off, and the water layer was extracted with chloroform. The chloroform layer was combined with the organic layer, and the combined organic layer was washed with 2N aqueous hydrochloric acid solution and dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure, and the residue was suspended in a mixture of 50 ml of saturated aqueous sodium hydrogencarbonate solution and 50 ml of methanol, and the resulting suspension was heated under reflux for 2 hours. The suspension was concentrated under reduced pressure, and water was added to the residue. The resulting mixture was extracted with ethyl acetate, and the extract was dried over anhydrous magnesium sulfate. The residue was concentrated under reduced pressure, and was recrystallized to afford 1.54 g of the desired product.

WORKUP

后处理

  1. customas obtained in Reference Example 2
  2. customThe organic layer was separated off
  3. extractionthe water layer was extracted with chloroform
  4. washthe combined organic layer was washed with 2N aqueous hydrochloric acid solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. concentrationThe organic layer was concentrated under reduced pressure
  7. additionthe residue was suspended in a mixture of 50 ml of saturated aqueous sodium hydrogencarbonate solution and 50 ml of methanol
  8. temperaturethe resulting suspension was heated
  9. temperatureunder reflux for 2 hours
  10. concentrationThe suspension was concentrated under reduced pressure, and water
  11. additionwas added to the residue
  12. extractionThe resulting mixture was extracted with ethyl acetate
  13. dry with materialthe extract was dried over anhydrous magnesium sulfate
  14. concentrationThe residue was concentrated under reduced pressure
  15. customwas recrystallized