Reacción #446435

ord-365598da8dfa4a518c5c99307f72946e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturais heated to +80° C
  2. 2
    Temperaturathe solution is cooled to +7° C.
  3. 3
    ExtracciónThe solution is extracted twice
  4. 4
    Secadothe organic phase is dried over sodium sulfate
  5. 5
    Concentraciónconcentrated to dryness by evaporation
  6. 6
    workup.ADDITIONis added
  7. 7
    FiltraciónThe resulting suspension is filtered
  8. 8
    Concentraciónthe filtrate is concentrated by evaporation
  9. 9
    Otrothe residue is crystallised from an ether/hexane mixture

Procedimiento

A mixture of 30.0 g of 1-(2,2-dimethylindan-1-yl)-5-imidazolecarboxylic acid methyl ester, 150 ml of water and 17 g of sulfuric acid is heated to +80° C. Within a period of 1.5 hours a solution of 114 g of ammonium peroxodisulfate is added dropwise thereto. When the reaction is complete, the solution is cooled to +7° C. and adjusted to pH 3 by the addition of 30% sodium hydroxide solution. The solution is extracted twice using 200 ml of methylene chloride each time, and the organic phase is dried over sodium sulfate and concentrated to dryness by evaporation. The residue is taken up in a small amount of methylene chloride, and ether is added. The resulting suspension is filtered, the filtrate is concentrated by evaporation and the residue is crystallised from an ether/hexane mixture. 19 g of 1-(2,2-dimethyl-3-oxoindan-1-yl)-5-imidazolecarboxylic acid methyl ester having a melting point of 104°-108° C. are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05000777uspto-grants-1991_03