Réaction #96167

ord-4d0cc944adab44b2ab2aa844f16512e8

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe reaction mixture is refluxed under nitrogen atmosphere for 30 minitres
  2. 2
    Températurecooled
  3. 3
    Autreevaporated to dryness
  4. 4
    Extractionof water and the resultant mixture extracted with ethyl acetate (2×50 ml.)
  5. 5
    SéchageThe combined extracts are dried over magnesium sulfate
  6. 6
    Autreevaporated to dryness under reduced pressure
  7. 7
    AutreCrystallization of the residue from ethyl acetate-hexane

Mode opératoire

A solution of 336 mg. of isopropyl 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]-pyrrole-1-carboxylate in 10 ml. of methanol is treated with a solution of 690 mg. of potassium carbonate in 5 ml. of water. The reaction mixture is refluxed under nitrogen atmosphere for 30 minitres, cooled, and evaporated to dryness. The residue is taken up in 10 ml. of 10% aqueous hydrochloric acid and 50 ml. of water and the resultant mixture extracted with ethyl acetate (2×50 ml.). The combined extracts are dried over magnesium sulfate and evaporated to dryness under reduced pressure. Crystallization of the residue from ethyl acetate-hexane affords 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04347185uspto-grants-1982_08