Réaction #45946

ord-d607a5691d4945faa36d1f0ad5c72ab5

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe reaction mixture was then filtered
  2. 2
    Autreto remove the catalyst
  3. 3
    AutreThe solvent was removed in vacuuo

Mode opératoire

The nitro intermediate (2 mmol) obtained above was dissolved in MeOH (10 mL) and hydrogenated in the presence of 10% Pd/C (50 mg) until completion as indicated by TLC or LC-MS, according to General Procedure H. The reaction mixture was then filtered to remove the catalyst. The solvent was removed in vacuuo to afford 4-(4′-fluoro-3′-trifluoromethyl-phenoxy)aniline, which was used directly for further transformation without purification (overall yield: 95%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07737285B2uspto-grants-2010_06