Реакция #88208

ord-2781ce35c46f4b819672aab6953c86b7

Реагенты

Нет

Растворители

Условия реакции

Температура
5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеfitted with a condenser
  2. 2
    Другоеwas removed from the reaction mixture
  3. 3
    ТемператураThe reaction was cooled
  4. 4
    Концентрированиеconcentrated
  5. 5
    workup.DISSOLUTIONThe residue was dissolved in MeOH (120 mL)
  6. 6
    ТемператураThe reaction was slowly heated to reflux
  7. 7
    ТемператураAfter 2 h at reflux
  8. 8
    Температураthe reaction was cooled to room temperature
  9. 9
    Концентрированиеconcentrated
  10. 10
    workup.DISSOLUTIONThe residue was dissolved in EtOAc
  11. 11
    ПромывкаThe organic layer was washed (3×H2O and brine)
  12. 12
    Сушкаdried (Na2SO4)
  13. 13
    Концентрированиеconcentrated

Методика

p-Anisaldehyde (411 mmol), 4-methoxybenzylamine (411 mmol) and toluene (500 mL) were combined in a round bottomed flask fitted with a condenser and a Dean-Stark trap. The reaction was refluxed for 1 h during which water was removed from the reaction mixture. The reaction was cooled and concentrated. The residue was dissolved in MeOH (120 mL). The mixture was cooled to 5° C. and NaBH4 (205 mmol) was added in portions over 45 min. The reaction was slowly heated to reflux. After 2 h at reflux, the reaction was cooled to room temperature and concentrated. The residue was dissolved in EtOAc. The organic layer was washed (3×H2O and brine), dried (Na2SO4) and concentrated to yield the desired product.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09440929B2uspto-grants-2016_09