Reacción #452423

ord-87c39bdb789b4bd292d5640130fc82a7

Ecuación de reacción

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
Rendimiento 91.3%

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06126932uspto-grants-2000_10