HRID4751

反应详情

EQUATION

反应方程式

HRID 4751 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 15 g (0.05 mole) 2-methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]benzaldehyde in 50 ml of pyridine are added 11 g (0.11 mole) of malonic acid and 1 g of piperidine. The solution is stirred and gradually heated to 80°. Heating and stirring are continued for 1 hour at 80°. The solution is then heated at reflux for an additional 3 hours, cooled, and evaporated at reduced pressure to obtain a residual oil which is extracted into ether. The resulting ether solution is washed with water and 1N hydrochloric acid, dried with anhydrous magnesium sulfate, filtered, and evaporated at reduced pressure to obtain a residual solid which is recrystallized from chlorobutane/hexane mixed solvent to give 10.5 g of 3-{2 -methoxy-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid having a melting point of 138°-140°.

WORKUP

后处理

  1. temperaturegradually heated to 80°
  2. temperatureHeating
  3. stirringstirring
  4. temperatureThe solution is then heated
  5. temperatureat reflux for an additional 3 hours
  6. temperaturecooled
  7. customevaporated at reduced pressure
  8. customto obtain a residual oil which
  9. extractionis extracted into ether
  10. washThe resulting ether solution is washed with water and 1N hydrochloric acid
  11. dry with materialdried with anhydrous magnesium sulfate
  12. filtrationfiltered
  13. customevaporated at reduced pressure
  14. customto obtain a residual solid which
  15. customis recrystallized from chlorobutane/hexane mixed solvent