HRID1087890

反应详情

EQUATION

反应方程式

HRID 1087890 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a stirred solution of 5.0 grams (0.029 mole) of 2-fluoroethyl 4-hydroxymethylphenyl ether in 50 ml of tetrahydrofuran was added 15 ml of a 50% aqueous, sodium hydroxide solution, 7.6 grams (0.060 mole) of 1-bromo-2-fluoroethane, and 0.78 gram (0.0023 mole) of tetrabutylammonium hydrogen sulfate. The resultant mixture was stirred and heated at reflux for approximately 18 hours. The mixture was cooled and was extracted with diethyl ether. The extract was washed in succession with a dilute, aqueous, sodium hydroxide solution, an aqueous 10% lithium chloride solution, and a saturated, aqueous, sodium chloride solution. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to leave an oil. Analysis of this oil by nmr indicated a large amount of starting material remained. The oil was again heated at reflux with the same quantities of the above reactants for 30 minutes. The reaction mixture was cooled and extracted with diethyl ether. The extract was washed several times with water followed by an aqueous, 15% lithium chloride solution. The washed extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure leaving an oil. Analysis of this oil by nmr indicated starting material was still present. This oil was heated at reflux with the same quantities of the above reagents for approximately 24 hours. The mixture was cooled and extracted with diethyl ether. The extract was washed with water and was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.9 grams of 4-(2-fluoroethoxymethyl)phenyl 2-fluoroethyl ether as an oil.

WORKUP

后处理

  1. temperatureheated
  2. temperatureat reflux for approximately 18 hours
  3. temperatureThe mixture was cooled
  4. extractionwas extracted with diethyl ether
  5. washThe extract was washed in succession with a dilute
  6. dry with materialThe washed organic phase was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customThe filtrate was evaporated under reduced pressure
  9. customto leave an oil
  10. temperatureThe oil was again heated
  11. temperatureat reflux with the same quantities of the above reactants for 30 minutes
  12. temperatureThe reaction mixture was cooled
  13. extractionextracted with diethyl ether
  14. washThe extract was washed several times with water
  15. extractionThe washed extract
  16. dry with materialwas dried over anhydrous magnesium sulfate
  17. filtrationfiltered
  18. customThe filtrate was evaporated under reduced pressure
  19. customleaving an oil
  20. temperatureThis oil was heated
  21. temperatureat reflux with the same quantities of the above reagents for approximately 24 hours
  22. temperatureThe mixture was cooled
  23. extractionextracted with diethyl ether
  24. washThe extract was washed with water
  25. dry with materialwas dried over anhydrous magnesium sulfate
  26. filtrationfiltered
  27. customThe filtrate was evaporated under reduced pressure