تفاعل #4838

معادلة التفاعل

acetic anhydride

4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]toluene

sulfuric acid

acetic anhydride

→

α,α -bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene

المذيبات

water

water

ظروف التفاعل

المعالجة

1. 1
   workup.STIRRINGAfter stirring
2. 2
   أخرىthe resulting reaction mixture
3. 3
   أخرىto obtain an aqueous mixture which
4. 4
   workup.WAITto stand for 18 hours
5. 5
   أخرىWater is decanted from the oily solid
6. 6
   workup.DISSOLUTIONThe solid is dissolved in ether
7. 7
   أخرىto obtain a solution which
8. 8
   غسيلis washed with water and sodium bicarbonate solution
9. 9
   تجفيفdried with anhydrous magnesium sulfate
10. 10
    ترشيحfiltered
11. 11
    أخرىevaporated at reduced pressure
12. 12
    أخرىto give an oily solid
13. 13
    أخرىThe solid is triturated with ether
14. 14
    ترشيحfiltered
15. 15
    أخرىrecrystallized from chlorobutane

الإجراء التجريبي

To a solution of 156 g (0.60 mole) of 4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]toluene in 675 ml of acetic anhydride is added 135 ml of concentrated sulfuric acid at 0°. To the solution stirred at 0° is added a soluton of 168 g (1.68 mole) of chromium trioxide in 750 ml of acetic anhydride dropwise over a two-hour period. After stirring is continued for an additional two hours, the resulting reaction mixture is poured into five liters of ice and is diluted with five liters of water to obtain an aqueous mixture which is allowed to stand for 18 hours. An oily solid with water above it is obtained. Water is decanted from the oily solid. The solid is dissolved in ether to obtain a solution which is washed with water and sodium bicarbonate solution, dried with anhydrous magnesium sulfate, filtered and evaporated at reduced pressure to give an oily solid. The solid is triturated with ether, filtered and recrystallized from chlorobutane to give 60 g of α,α -bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene, m.p. 93°-94.6°.

المصدر