Réaction #992748

ord-4ab46b4b5a40475ab86c1d8416bb67e7

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationfiltered
  2. 2
    workup.ADDITIONWater (100 mL) was added
  3. 3
    Extractionthe mixture was extracted with ethyl acetate (2×100 mL)
  4. 4
    LavageThe combined organic phases were washed with water (2×200 mL) and brine (200 mL)
  5. 5
    Séchagedried over sodium sulfate
  6. 6
    Concentrationconcentrated in vacuo

Mode opératoire

Aqueous hydrochloric acid (2 M, 45 mL) was added slowly to a mixture of zinc dust (8.6 g) and 2-bromo-4-nitro-6-trifluoromethyl-phenylamine (2.5 g) in tetrahydrofuran (50 mL). The reaction mixture was stirred for 1 hour, filtered and neutralized with saturated aqueous sodium bicarbonate (100 mL). Water (100 mL) was added and the mixture was extracted with ethyl acetate (2×100 mL). The combined organic phases were washed with water (2×200 mL) and brine (200 mL), dried over sodium sulfate and concentrated in vacuo to furnish 2.22 g (98% yield) of the title compound as a red solid. 1H NMR (500 MHz, DMSO-d6): 4.55 (s, 2H), 4.91 (s, 2H), 6.76 (d, 1H), 7.01 (d, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08012962B2uspto-grants-2011_09