Reaktion #942126

ord-6866e5a6de484416ab4982b43116b460

Reaktionsgleichung

Cc1cc(Cl)cc2c1NC(=O)C2=O
5-chloro-7-methyl-1H-indole-2,3-dione
[K+].[OH-]
potassium hydroxide
OO
hydrogen peroxide
CCOC(C)=O
ethyl acetate
Cc1cc(Cl)cc(C(=O)O)c1N
2-amino-5-chloro-3-methylbenzoic acid

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with I N hydrochloric acid (3×200 mL)
  2. 2
    TrocknenThe solution was dried over sodium sulfate and solvent
  3. 3
    Sonstigeremoved at reduced pressure

Vorschrift

The 5-chloro-7-methyl-1H-indole-2,3-dione (25.0 g, 0.13 mol), potassium hydroxide (8.4 g, 0.15 mmol) and 30% hydrogen peroxide (21.6 g, 0.18 mol) were mixed together in methanol (300 mL) at 0° C. for 2 h followed by 16 h at room temperature. The solution was poured into ethyl acetate (500 mL) and extracted with I N hydrochloric acid (3×200 mL) followed by brine (1×50 mL). The solution was dried over sodium sulfate and solvent removed at reduced pressure. The 2-amino-5-chloro-3-methylbenzoic acid (18.0 g, 0.10 mmol) was isolated as a yellow solid (75% yield). HRMS m/z 185.0238; calcd 185.0244.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07259266B2uspto-grants-2007_08