Reaktion #56946

ord-117d740f4ce941b198f1a4abcf68544e

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturat reflux under argon for 24 h
  2. 2
    EinengenThe suspension was concentrated under reduced pressure
  3. 3
    Sonstigethe residue was sonicated with 1M HCl (aq) over 1.5 h
  4. 4
    SonstigeThe resultant orange solid was isolated by filtration
  5. 5
    Waschenwashed with water
  6. 6
    Sonstigedried
  7. 7
    Sonstigesonicated with t-butyl methyl ether
  8. 8
    Sonstigeisolated by filtration
  9. 9
    Sonstigedried
  10. 10
    SonstigeWhere necessary, the product was further purified by recrystallisation

Vorschrift

4-Fluoro-3-nitrobenzoic acid (0.27 mol), an aniline (0.32 mol) and NMM (32.5 mL) in 2-methoxyethanol (750 mL) were stirred at reflux under argon for 24 h. The suspension was concentrated under reduced pressure and the residue was sonicated with 1M HCl (aq) over 1.5 h. The resultant orange solid was isolated by filtration, washed with water dried, then sonicated with t-butyl methyl ether, isolated by filtration and dried. Where necessary, the product was further purified by recrystallisation to yield the 4-anilino-3-nitrobenzoic acid: e.g. 4-(3-bromophenyl amino)-3-nitrobenzoic acid. (In some cases, for example with heteroaromatic anilines, NMN may be omitted from the reaction mixture).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07419995B2uspto-grants-2008_09