تفاعل #56946

ord-117d740f4ce941b198f1a4abcf68544e

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةat reflux under argon for 24 h
  2. 2
    تركيزThe suspension was concentrated under reduced pressure
  3. 3
    أخرىthe residue was sonicated with 1M HCl (aq) over 1.5 h
  4. 4
    أخرىThe resultant orange solid was isolated by filtration
  5. 5
    غسيلwashed with water
  6. 6
    أخرىdried
  7. 7
    أخرىsonicated with t-butyl methyl ether
  8. 8
    أخرىisolated by filtration
  9. 9
    أخرىdried
  10. 10
    أخرىWhere necessary, the product was further purified by recrystallisation

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07419995B2uspto-grants-2008_09