Réaction #992747

ord-5002d1daa15c45d79ff37db84186b41a

Conditions de réaction

Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationfiltered
  2. 2
    LavageThe collected solid was washed with water (200 mL)
  3. 3
    Autredried in vacuo

Mode opératoire

Bromine (0.60 mL) dissolved in acetic acid (11 mL) was added dropwise to a solution of 4-nitro-2-trifluoromethyl-phenylamine (2.4 g) in acetic acid (12 mL). The reaction mixture was heated to 120° C. for 2½ hours, poured into water (400 mL) and filtered. The collected solid was washed with water (200 mL) and dried in vacuo to furnish 3.03 g (91% yield) of the title compound as a yellow solid. 1H NMR (500 MHz, DMSO-d6): 7.08 (s, 2H), 8.23 (d, 1H), 8.51 (d, 1H).

Source

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