反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- temperaturegradually heated to 80°
- temperatureHeating
- stirringstirring
- temperatureThe solution is then heated
- temperatureat reflux for an additional 3 hours
- temperaturecooled
- customevaporated at reduced pressure
- customto obtain a residual oil which
- extractionis extracted into ether
- washThe resulting ether solution is washed with water and 1N hydrochloric acid
- dry with materialdried with anhydrous magnesium sulfate
- filtrationfiltered
- customevaporated at reduced pressure
- customto obtain a residual solid which
- customis recrystallized from chlorobutane/hexane mixed solvent