Reacción #93502

ord-6072f8e986394fa2bd99331cd89b6304

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturachill in the refrigerator overnight
  2. 2
    Otrothe progress of the reaction by thin-layer chromatography on silica gel (acetonitrile: ammonium hydroxide, 90:10)
  3. 3
    OtroAt the completion of the reaction
  4. 4
    ExtracciónExtract the aqueous mixture with 3×300 ml ether
  5. 5
    LavadoWash the combined organic layers with 1N hydrochloric acid
  6. 6
    Secadowith water, dry over potassium carbonate
  7. 7
    Filtraciónfilter
  8. 8
    Otroremove the solvent in vacuo

Procedimiento

To a 0° C. solution of 4.5 g (0.022 mole) 4-(acetylamino)benzenebutanol in 25 ml pyridine, add 8.3 g (0.044 mole) tosyl chloride and chill in the refrigerator overnight. Follow the progress of the reaction by thin-layer chromatography on silica gel (acetonitrile: ammonium hydroxide, 90:10). At the completion of the reaction, pour the reaction mixture onto 500 ml ice water and stir for 15 minutes. Extract the aqueous mixture with 3×300 ml ether. Wash the combined organic layers with 1N hydrochloric acid, then with water, dry over potassium carbonate, filter and remove the solvent in vacuo to obtain the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04613609uspto-grants-1986_09