反应详情

In a three neck flask purged with nitrogen were charged magnesium (12.2 g, 502 mmol) and ether (100 ml). A solution of 4-bromotoluene (56.1 ml, 456 mmol) in ether (200 ml) was added dropwise, and the mixture was heated under reflux for 1.5 hrs. The reaction vessel was cooled in a dry ice-acetone bath. A solution of pentafluoropropionic acid (25 g, 152 mmol) in ether (100 ml) was added dropwise, and the temperature was slowly raised to room temperature. The mixture was heated under reflux for 3 hrs, and stirred overnight at room temperature. The reaction mixture was ice-cooled, and quenched with 3N hydrochloric acid. The mixture was diluted with ethyl acetate, and the organic layer was separated and washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:0, 30:1) to give a colorless transparent oil. This was dissolved in methanol, and sodium borohydride was added under ice-cooling. The temperature was raised to, room temperature, and the mixture was stirred for 1 hr. After completion of the reaction, the reaction was quenched with 6N hydrochloric acid, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1, 5:1) to give 2,2,3,3,3-pentafluoro-1-(4-methylphenyl)propan-1-ol (20.28 g, 56%) as a colorless transparent oil.

1. customIn a three neck flask purged with nitrogen
2. temperaturethe mixture was heated
3. temperatureunder reflux for 1.5 hrs
4. temperatureThe reaction vessel was cooled in a dry ice-acetone bath
5. temperatureThe mixture was heated
6. temperatureunder reflux for 3 hrs
7. temperaturecooled
8. customquenched with 3N hydrochloric acid
9. additionThe mixture was diluted with ethyl acetate
10. customthe organic layer was separated
11. washwashed with saturated aqueous sodium hydrogen carbonate and saturated brine
12. dry with materialdried over anhydrous magnesium sulfate
13. filtrationfiltered
14. concentrationconcentrated under reduced pressure
15. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:0, 30:1)
16. customto give a colorless transparent oil
17. temperaturecooling
18. temperatureThe temperature was raised to, room temperature
19. stirringthe mixture was stirred for 1 hr
20. customAfter completion of the reaction
21. customthe reaction was quenched with 6N hydrochloric acid
22. extractionthe mixture was extracted with ethyl acetate
23. washThe organic layer was washed with saturated brine
24. dry with materialdried over anhydrous magnesium sulfate
25. filtrationfiltered
26. concentrationconcentrated under reduced pressure
27. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1, 5:1)