Реакция #67615

ord-d3b48ac36ef04da0a64fbe747cc56d37

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    workup.ADDITIONThe mixture was poured onto ice water (200 ml)
  3. 3
    Экстракцияextracted with EtOAc (×6)
  4. 4
    ПромывкаThe combined extracts were washed with brine
  5. 5
    Сушкаdried over MgSO4
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated
  8. 8
    ФильтрацияTritration with ether followed by filtration

Методика

3-Methyl-4-nitrobenzoic acid (3.0 g, 16.56 mmol) in DMF (30 mL) was stirred with carbonyl diimidazole (3.22 g, 1.2 Eq.) for 90 mins. The reaction mixture was cooled in an icebath, and dimethylamine (2 M in THF, 25 mL, 3 Eq.) was added. The mixture was then allowed to warm to room temperature and stirred for 2 hours. The mixture was poured onto ice water (200 ml) and extracted with EtOAc (×6). The combined extracts were washed with brine, dried over MgSO4, filtered and evaporated. Tritration with ether followed by filtration gave N,N,3-trimethyl-4-nitrobenzamide (2.6 g, colourless solid); MS (ES+) 209.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524902B2uspto-grants-2013_09