Реакция #1687153

ord-f491c729248d4d28947c17fd6ee5332d

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONare added
  2. 2
    ТемператураThe mixture is then heated
  3. 3
    Другоеthus obtained
  4. 4
    Температураandthe mixture is subsequently refluxed for a further 3 hours
  5. 5
    Экстракцияis extracted with methylene chloride
  6. 6
    ДругоеAfter drying
  7. 7
    Концентрированиеthe organic phase is concentrated
  8. 8
    ДругоеThe solid obtained
  9. 9
    Другоеis sufficiently pure for the subsequent reaction (NMR)

Методика

49.7 g (0.253 mol) of 2-methyl-3-nitro-6-aminobenzoic acid are dissolved in380 ml of acetone and 43 g (0.51 mol) of sodium hydrogen carbonate are added. The mixture is then heated to boiling until evolution of CO2 is complete. 35.3 g (0.28 mol) of dimethyl sulfate are then added in the course of two hours at the boiling point of acetone to the suspension of the sodium salt of 2-methyl-3-nitro-6-aminobenzoic acid thus obtained, andthe mixture is subsequently refluxed for a further 3 hours and then allowedto cool. After pouring the reaction mixture into 1.8 l of water, it is extracted with methylene chloride. After drying, the organic phase is concentrated. The solid obtained is sufficiently pure for the subsequent reaction (NMR). Yield: 50 g (0.238 mol)=94% of theory, m.p.: 92°-94° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05744425uspto-grants-1998_04