HRID71903

反应详情

EQUATION

反应方程式

HRID 71903 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A solution of TFAA (2.1 mL, 3.15 mmol) in dichloromethane (5 mL) was added dropwise to a suspension of 2,7-dibromo-fluoren-9-one (3.3 g, 10 mmol) and H2O2-urea (1.4 g, 15 mL) in dichloromethane (50 mL). The mixture was stirred at room temperature for 48 hours, a second portion of H2O2-urea was added, and stirring was continued at room temperature for a further 72 hours. The mixture was filtered, the organic phase was extracted with water (50 mL), and dried over Na2SO4. After removal of solvent, the residue was heated with 2N NaOH at 80° C. for 10 minutes, filtered, the cooled filtrate extracted with ether. The aqueous phase was acidified with 2N HCl and extracted with ethyl acetate (200 mL). HCl (2 mL 4M solution) was added to the ethyl acetate and heated for 2 hours. The solvent was removed under vacuum, the residue was recrystallized from ethyl acetate/ethanol to give the final product 3,8-Dibromo-benzo[c]chromen-6-one as a white solid (1.5 g, 40%).

WORKUP

后处理

  1. stirringstirring
  2. waitwas continued at room temperature for a further 72 hours
  3. filtrationThe mixture was filtered
  4. extractionthe organic phase was extracted with water (50 mL)
  5. dry with materialdried over Na2SO4
  6. customAfter removal of solvent
  7. temperaturethe residue was heated with 2N NaOH at 80° C. for 10 minutes
  8. filtrationfiltered
  9. extractionthe cooled filtrate extracted with ether
  10. extractionextracted with ethyl acetate (200 mL)
  11. additionHCl (2 mL 4M solution) was added to the ethyl acetate
  12. temperatureheated for 2 hours
  13. customThe solvent was removed under vacuum
  14. customthe residue was recrystallized from ethyl acetate/ethanol