Реакция #7239

ord-b0ed2b81d0864736adc41f19e2b2dd94

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe solution was heated at 70° C. overnight
  2. 2
    Температураto cool to room temperature
  3. 3
    Концентрированиеconcentrated under reduced pressure
  4. 4
    workup.DISSOLUTIONThe residue was dissolved in CHCl3 (100 mL)
  5. 5
    workup.ADDITIONtreated with solid Na2CO3 (14.12 g)
  6. 6
    workup.WAITAfter 1 hour
  7. 7
    Другоеthe supernatant was decanted
  8. 8
    Промывкаthe residue was washed with warm CHCl3 (3×50 mL)
  9. 9
    ФильтрацияThe combined supernatants were filtered
  10. 10
    Концентрированиеconcentrated
  11. 11
    Другоеto provide 4.6951 g as a yellow solid
  12. 12
    Температураheated at 90° C. overnight
  13. 13
    ТемператураThe mixture was cooled to room temperature
  14. 14
    Концентрированиеconcentrated
  15. 15
    Фильтрацияthe crude product was filtered through a silica plug (33 g silica, ethyl acetate)

Методика

To a stirred solution of 2,3-lutidine (4.8363 g, 45.13 mmol) in glacial acetic acid (30 mL) at room temperature was added 30% H2O2 (4.6 mL) and the resultant solution was heated to 70° C. After 6 hours, the reaction mixture was cooled to room temperature, additional H2O2 (4.6 mL) was added, and the solution was heated at 70° C. overnight. The reaction mixture was allowed to cool to room temperature and then concentrated under reduced pressure. The residue was dissolved in CHCl3 (100 mL) and treated with solid Na2CO3 (14.12 g). After 1 hour, the supernatant was decanted and the residue was washed with warm CHCl3 (3×50 mL). The combined supernatants were filtered and concentrated to provide 4.6951 g as a yellow solid. The solid was dissolved in acetic anhydride (38 mL) and heated at 90° C. overnight. The mixture was cooled to room temperature and concentrated and the crude product was filtered through a silica plug (33 g silica, ethyl acetate) to give 6.13 g of 2-acetoxymethyl-3-methyl-pyridine as an orange oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07084155B2uspto-grants-2006_08