تفاعل #4840

ord-d619ebd614624d4388075e24b6d34182

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting reaction mixture
  2. 2
    أخرىthe reaction
  3. 3
    أخرىThe solvent can be removed
  4. 4
    workup.DISSOLUTIONthe residual oil dissolved in ether
  5. 5
    أخرىto obtain an ether solution which
  6. 6
    استخلاصcan be extracted with 1N hydrochloride acid
  7. 7
    درجة الحرارةThe resulting sodium hydroxide solution can be heated on the steam bath
  8. 8
    درجة الحرارةcooled
  9. 9
    أخرىto obtain a product which
  10. 10
    تجفيفThe resulting ether solution can be dried with anhydrous magnesium sulfate
  11. 11
    ترشيحfiltered
  12. 12
    أخرىevaporated

الإجراء التجريبي

To a solution of methyl 3-bromo-3-methyl-{4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}propanoate in tetrahydrofuran can be added an equivalent amount of 1,5-diazabicyclo[3.4.0]nonene-5. The resulting reaction mixture can be stirred at elevated temperature until thin layer chromatographic analysis of a reaction sample indicates the reaction to be complete. The solvent can be removed and the residual oil dissolved in ether to obtain an ether solution which can be extracted with 1N hydrochloride acid and then by 2N sodium hydroxide solution. The resulting sodium hydroxide solution can be heated on the steam bath, cooled and made acidic with concentrated hydrochloric acid to obtain a product which can be isolated from the aqueous phase with ether. The resulting ether solution can be dried with anhydrous magnesium sulfate, filtered, and evaporated to give 3-methyl-3-{4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl}-2-propenoic acid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04727180uspto-grants-1988_02