تفاعل #50769

ord-01a5608ff8024c5eb682c47225811f55

معادلة التفاعل

O=[N+]([O-])c1ccccc1F
2-fluoronitrobenzene
Nc1ccc(I)cc1
4-iodoaniline
CCN(CC)CC
triethylamine
O=[N+]([O-])c1ccccc1Nc1ccc(I)cc1
N-(4-iodophenyl)-2-nitroaniline
المردود 48.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةunder reflux
  3. 3
    درجة الحرارةto cool
  4. 4
    غسيلThe solution was washed with water (2×100 ml), aqueous 2M potassium hydroxide (100 ml) and brine (100 ml)
  5. 5
    تجفيفThe organics were dried over anhydrous magnesium sulphate
  6. 6
    أخرىthe solvent removed under reduced pressure
  7. 7
    أخرىto give an orange solid
  8. 8
    أخرىRecrystalisation from ethyl acetate

الإجراء التجريبي

A mixture of 2-fluoronitrobenzene (14 g, 100 mmol), 4-iodoaniline (11 g, 50 mmol) and triethylamine (14 ml, 100 mmol) was heated under reflux. After 48 h the reaction mixture was allowed to cool and ethyl acetate (300 ml) was added. The solution was washed with water (2×100 ml), aqueous 2M potassium hydroxide (100 ml) and brine (100 ml). The organics were dried over anhydrous magnesium sulphate and the solvent removed under reduced pressure to give an orange solid. Recrystalisation from ethyl acetate gave N-(4-iodophenyl)-2-nitroaniline (8.2 g, 48%) as an orange crystalline solid. deltaH (250 MHz, CDCl3) 9.39 (1H, s), 8.21 (1H, dd, J 8.5, 1.5 Hz), 7.71 (2H, dd, J 8.6, 2.0 Hz), 7.39 (1H, m), 7.24 (1H, m), 7.05 (2H, dd, J 8.6, 1.4 Hz), 6.83 (1H, m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05428168uspto-grants-1995_06