Реакция #67708

ord-2e1ade2d28d9474d8de193c5da09005f

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvents were evaporated off
  2. 2
    Экстракцияextracted twice with tert-butyl methyl ether
  3. 3
    workup.ADDITIONThe aqueous phase was adjusted to pH 2 by addition of 25% HCl
  4. 4
    Экстракцияextracted twice with tert-butyl methyl ether
  5. 5
    ДругоеThe combined organic phases were dried on sodium sulfate
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated
  8. 8
    ДругоеThe crude material, off-white solid (1.01 g, 54%) was used without further purification

Методика

Crude 2-cyclopropyl-4,6-bis-trifluoromethyl-benzaldehyde (intermediate 0, 1.01 g, 3.58 mmol) was dissolved in 8.5 mL tert-butylalcohol and 4.5 mL 2-methyl-2-butene. At 0° C. a solution of sodium chlorite (340 mg, 3.76 mmol) and sodium dihydrogenphosphat (451 mg, 3.76 mmol) in 3 mL water was added. The reaction mixture was stirred at room temperature overnight. The solvents were evaporated off. The residue was taken up in 1N NaOH and extracted twice with tert-butyl methyl ether. The aqueous phase was adjusted to pH 2 by addition of 25% HCl and extracted twice with tert-butyl methyl ether. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The crude material, off-white solid (1.01 g, 54%) was used without further purification.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524909B2uspto-grants-2013_09