تفاعل #84240

ord-1a95de0f49494be9891b705ba09698b7

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGwhile the solution was stirred for 20 min.
  2. 2
    workup.STIRRINGto stir overnight (16 hrs)
  3. 3
    تركيزThe reaction mixture was concentrated in vacuo
  4. 4
    أخرىtriturated with hexanes (3×400 mL)
  5. 5
    تركيزconcentrated to dryness
  6. 6
    workup.DISSOLUTIONThe crude solid was dissolved in diethyl ether (400 mL)
  7. 7
    غسيلwashed with water (3×)
  8. 8
    workup.ADDITIONthe organic extracts were diluted with hexanes (400 mL)
  9. 9
    أخرىa white solid precipitated
  10. 10
    ترشيحThe solid was filtered
  11. 11
    أخرىdried in a vacuum oven (35° C. @ 762 Torr) overnight

الإجراء التجريبي

4-Amino-2-trifluoromethyl-benzonitrile (20.44 g, 109.79 mmoles) and p-toluenesulfonic acid monohydrate (1.05 g, 5.52 mmoles) were dissolved methanol (200 mL) and THF (200 mL), and the reaction mixture was stirred under a nitrogen atmosphere. The reaction vessel was wrapped in aluminium foil, while the solution was stirred for 20 min., then N-iodosuccinimide (30.41 g, 135.17 mmoles) was added and the reaction was allowed to stir overnight (16 hrs). The reaction mixture was concentrated in vacuo, triturated with hexanes (3×400 mL) and concentrated to dryness. The crude solid was dissolved in diethyl ether (400 mL), washed with water (3×), the organic extracts were diluted with hexanes (400 mL) and a white solid precipitated. The solid was filtered and dried in a vacuum oven (35° C. @ 762 Torr) overnight to yield the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09434688B2uspto-grants-2016_09