Réaction #50463

ord-1a2558a25c3149839e0db0e3cae5a089

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autreover 10 minutes
  2. 2
    workup.ADDITIONpoured
  3. 3
    Autreover crushed ice
  4. 4
    ExtractionThe suspension was extracted 3× with ethyl acetate
  5. 5
    LavageThe combined organic extracts were washed 1× with water
  6. 6
    Séchagedried over MgSO4
  7. 7
    Concentrationconcentrated in vacuo
  8. 8
    AutreThere was obtained a dark oil, which
  9. 9
    Autreupon standing at room temperature

Mode opératoire

To a solution of 1.0 g (4.5 mmoles) of 5-nitro-4-ethylisatin in 8.0 mL of 5% NaOH was slowly added 1.25 mL (11 mmoles) of 30% hydrogen peroxide over 10 minutes. A mild exotherm was detectable. The solution was stirred at room temperature for 60 minutes, then poured over crushed ice. The solution was acidified with 10% HCl until the `cloud point`. The suspension was extracted 3× with ethyl acetate. The combined organic extracts were washed 1× with water, dried over MgSO4, and concentrated in vacuo. There was obtained a dark oil, which upon standing at room temperature, became an orange-rust colored solid. 0.78 g (82% yield) of 5-nitro-6-ethyl-2-aminobenzoic acid was obtained. NMR(DMSO-d6): 1.16(t,3H,J=7.2 Hz), 2.88(q,2H,J=7.2 Hz), 3.34(bs,2H), 6.66(d,1H,J=9.3 Hz), 7.84(d,1H,J=9.3 Hz). MS(m/z): 210(M+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05428021uspto-grants-1995_06