Reacción #1333841

ord-b8c559926c78449eb05d6aab792c8e98

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrosealed 350 mL round-bottomed pressure flask
  2. 2
    workup.ADDITIONcontaining
  3. 3
    Otrovia bubbling for 5 min through the septum
  4. 4
    Otrothe flask was then sealed
  5. 5
    TemperaturaThe solution was heated in an oil bath
  6. 6
    TemperaturaThe flask was cooled to room temperature
  7. 7
    ExtracciónThe aqueous layer was extracted with Et2O (3×200 mL)
  8. 8
    Secadothe combined organics were dried (Na2SO4)
  9. 9
    Filtraciónfiltered
  10. 10
    Concentraciónconcentrated in vacuo

Procedimiento

To a tared, sealed 350 mL round-bottomed pressure flask containing a suspension of 3,5-dibromophenol (10.0 g, 39.7 mmol; see step (ii) above) and Cs2CO3 (20.7 g, 63.5 mmol) in DMF (150 mL) at −78° C. was added chlorofluoromethane via bubbling for 5 min through the septum. The septum was replaced with a Teflon stopper and the flask was then sealed and allowed to warm to room temperature where the flask was weighed and determined to contain 9.0 g (131 mmol) of chlorofluoromethane. The solution was heated in an oil bath set at 70° C. overnight. The flask was cooled to room temperature, the pressure cautiously released and the contents diluted with water (100 mL). The aqueous layer was extracted with Et2O (3×200 mL) then, the combined organics were dried (Na2SO4), filtered and concentrated in vacuo. Flash chromatography on silica gel eluting with hexanes afforded the sub-title compound. (7.9 g, 71%) as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07129233B2uspto-grants-2006_10