Реакция #452423

ord-87c39bdb789b4bd292d5640130fc82a7

Уравнение реакции

O
water
O=C(Cl)c1ccc(F)cc1
4-fluorobenzoyl chloride
Nc1ccc([N+](=O)[O-])cc1
4-nitroaniline
c1ccncc1
pyridine
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccc(F)cc1
N-(4-fluorobenzoyl)-4-nitroaniline
Выход 91.3%

Реагенты

Нет

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.WAITfor an hour at room temperature
  2. 2
    Другоеthe solid which formed
  3. 3
    Фильтрацияwas collected by filtration
  4. 4
    ПромывкаThe filter cake was washed with hexane (80 mL)
  5. 5
    Другоеwas then dried under vacuum at 60° C.

Методика

To a stirred suspension of 19.83 gm (143.56 mMol) 4-nitroaniline in 150 mL dichloromethane and 12.9 mL (159.5 mMol) pyridine at 0° C. were slowly added 24.5 gm (154.8 mMol) 4-fluorobenzoyl chloride. The reaction mixture was then stirred for 15 minutes at 0° C., at which time the reaction mixture became homogeneous, and then for an hour at room temperature. To this mixture were then added 100 mL water and the solid which formed was collected by filtration. The filter cake was washed with hexane (80 mL) followed by water (100 mL) and it was then dried under vacuum at 60° C. to give 34.1 gm (91%) N-(4-fluorobenzoyl)-4-nitroaniline.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06126932uspto-grants-2000_10