반응 #61222

ord-1fd312ac805b4dfeadac16093750d1c8

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07427682B2uspto-grants-2008_09