反応 #452423

ord-87c39bdb789b4bd292d5640130fc82a7

反応方程式

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
収率 91.3%

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITfor an hour at room temperature
  2. 2
    その他the solid which formed
  3. 3
    ろ過was collected by filtration
  4. 4
    洗浄The filter cake was washed with hexane (80 mL)
  5. 5
    その他was then dried under vacuum at 60° C.

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06126932uspto-grants-2000_10