Реакция #4359

ord-fa8aee38ba2a46708a7c9d020ef29ebe

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураwhile cooling with ice
  2. 2
    Другоеrises to 45°-50° C
  3. 3
    ТемператураThe mixture is then heated at 90°-100° C. for a further 3 hours
  4. 4
    Фильтрацияthe precipitate is filtered off with suction
  5. 5
    Промывкаwashed with water
  6. 6
    workup.DISSOLUTIONThe moist crude product is dissolved hot in 30 ml of methanol
  7. 7
    workup.ADDITION150 ml of H2O were added to the solution
  8. 8
    ФильтрацияThe precipitate is filtered off cold with suction
  9. 9
    Промывкаwashed with CH3OH/H2O
  10. 10
    Другоеdried in vacuo at 80° C

Методика

40 ml of concentrated nitric acid are added dropwise to 34 ml of concentrated sulphuric acid, while cooling with ice and stirring. 20.9 g of 2,4-dichloro-5-fluorobenzoic acid are introduced in portions into this nitration mixture, whereupon the temperature rises to 45°-50° C. The mixture is then heated at 90°-100° C. for a further 3 hours, the mixture is cooled to room temperature and poured onto 350 ml of ice-water and the precipitate is filtered off with suction and washed with water. The moist crude product is dissolved hot in 30 ml of methanol, and 150 ml of H2O were added to the solution. The precipitate is filtered off cold with suction, washed with CH3OH/H2O and dried in vacuo at 80° C. 21.2 g of crude 2,4-dichloro-5-fluoro-3-nitro-benzoic acid are obtained. The compound is sufficiently pure for the subsequent reactions. A sample recrystallized from toluene/petroleum ether gives crystals of melting point 192° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725595uspto-grants-1988_02