تفاعل #85154

ord-bd86b2b2b4b94a849ac3e96ea4f9d0ad

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction was subsequently terminated by addition of 10 ml of methanol
  2. 2
    workup.ADDITIONThe reaction mixture was diluted with 30 ml of aqueous 20% strength sodium potassium tartrate solution and 30 ml of aqueous buffer solution (pH 7)
  3. 3
    workup.STIRRINGstirred vigorously at room temperature overnight
  4. 4
    أخرىThe phases were separated
  5. 5
    استخلاصthe aqueous phase was extracted three times with dichloromethane
  6. 6
    تجفيفThe combined organic phases were dried over magnesium sulphate
  7. 7
    ترشيحfiltered
  8. 8
    أخرىthe solvent was removed under reduced pressure

الإجراء التجريبي

At 0° C., 26.7 ml (26.7 mmol) of diisobutylaluminum hydride (1M in dichloromethane) were slowly added dropwise to a solution of 1.89 g (10.7 mmol) of methyl 1-(trifluoromethyl)cyclopropanecarboxylate in 10 ml of dichloromethane. The mixture was then stirred at 0° C. for another 2 h and the reaction was subsequently terminated by addition of 10 ml of methanol. The reaction mixture was diluted with 30 ml of aqueous 20% strength sodium potassium tartrate solution and 30 ml of aqueous buffer solution (pH 7) and stirred vigorously at room temperature overnight. The phases were separated and the aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The crude product corresponded to the title compound. Yield: 0.96 g (64% of theory)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09434690B2uspto-grants-2016_09