Реакция #65383

ord-90fe87addf29438a8e3aa7aa6b4f105f

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияextracted with toluene
  2. 2
    ПромывкаThe organic layer was washed with 0.5 N aqueous sodium hydroxide solution and water in that order
  3. 3
    Сушкаdried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was distilled off
  5. 5
    ДругоеThe residue was chromatographed on a silica gel column and elution
  6. 6
    ДругоеThe Crystals from the eluate were recrystallized from 15 ml of hexane twice

Методика

To a mixture of 10 g of 2-nitro-4-trifluoromethylphenol, 8.0 g of anhydrous calcium carbonate and 30 ml of N,N-dimethylformamide was added dropwise a solution of 8.8 g of 2-bromoisobutyraldehyde in 23 ml of N,N-dimethylformamide and the mixture was stirred at room temperature for 4 days. The reaction mixture was then poured in ice-water and extracted with toluene. The organic layer was washed with 0.5 N aqueous sodium hydroxide solution and water in that order and dried over anhydrous magnesium sulfate and the solvent was distilled off. The residue was chromatographed on a silica gel column and elution was carried out with hexane-ethyl acetate (3:1). The Crystals from the eluate were recrystallized from 15 ml of hexane twice to give 4.428 g of 2-(2-nitro-4-trifluoromethylphenoxy)isobutyraldehyde.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05420126uspto-grants-1995_05