Реакция #465940

ord-d56a9f234b74453eaae79dd95b7cda1e

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in methanol (30 ml)
  3. 3
    workup.ADDITION2 N aqueous sodium hydroxide (20 ml) was added
  4. 4
    workup.STIRRINGthe mixture was stirred at room temperature for 2 hours
  5. 5
    КонцентрированиеAfter concentration, water
  6. 6
    workup.ADDITIONwas added to the residue
  7. 7
    Экстракцияthe mixture was extracted with ethyl acetate
  8. 8
    СушкаThe extract was dried over magnesium sulfate
  9. 9
    workup.DISTILLATIONthe solvent was then distilled off
  10. 10
    ПромывкаElution
  11. 11
    Другоеwith chloroform-methanol (10:1) and recrystallization from isopropyl ether

Методика

Concentrated sulfuric acid (2 drops) was added to a solution 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine-1-oxide (2.5 g) in acetic anhydride (8 ml) and the mixture was stirred at 110° C. for 2 hours and then concentrated. The residue was dissolved in methanol (30 ml), 2 N aqueous sodium hydroxide (20 ml) was added, and the mixture was stirred at room temperature for 2 hours. After concentration, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was then distilled off, and te residue was applied to a silica gel (50 g) column. Elution with chloroform-methanol (10:1) and recrystallization from isopropyl ether gave 1.6 g of 2-hydroxymethyl-3-methyl-4-(2,2,3,3, 3-pentafluoropropoxy)pyridine as a brown oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06296875B1uspto-grants-2001_10