Reacción #217752

ord-9b461631879345bd92daf1ca4edaa640

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaA glass flask with reflux condenser, heatable oil bath, mechanical stirrer
  2. 2
    workup.STIRRINGIt was stirred at 60° C. for one hour (the contents of the flask
  3. 3
    TemperaturaThen the reaction mixture was cooled
  4. 4
    workup.DISTILLATIONthe water was distilled off under reduced pressure, 20 mbar, at 30-45° C
  5. 5
    Otrowas taken up at 60° C. in 200 ml of toluene
  6. 6
    workup.DISTILLATIONSubsequently the mixture was redistilled
  7. 7
    OtroThe residue was recrystallized from 50 ml of butyl acetate
  8. 8
    FiltraciónThe product was filtered off
  9. 9
    Lavadowashed with butyl acetate
  10. 10
    Otrodried at 80° C.
  11. 11
    Otro10 mbar in a vacuum drying cabinet
  12. 12
    OtroThis gave a white solid

Procedimiento

A glass flask with reflux condenser, heatable oil bath, mechanical stirrer and internal thermometer was charged at room temperature with 35.90 g of ethyl salicylate and 282.13 g of water and these components were stirred together thoroughly. Subsequently 139.98 g of tetrabutylammonium hydroxide (40% strength in water) were added and the reaction mixture was heated to 60° C. It was stirred at 60° C. for one hour (the contents of the flask become clear). Then the reaction mixture was cooled and the water was distilled off under reduced pressure, 20 mbar, at 30-45° C. The residue was taken up at 60° C. in 200 ml of toluene. Subsequently the mixture was redistilled. The residue was recrystallized from 50 ml of butyl acetate. The product was filtered off, washed with butyl acetate and dried at 80° C. and 10 mbar in a vacuum drying cabinet. This gave a white solid having a melting point of 93° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07381785B2uspto-grants-2008_06