Reaktion #85459

ord-5cd1a66f188643dfa1d23e9527a7ee0b

Lösungsmittel

Reaktionsbedingungen

Temperatur
20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe temperature is increased to 30° C. for 1 hour
  2. 2
    Temperaturthen cooled to 20° C.
  3. 3
    Temperaturmaintaining the temperature at less than 30° C
  4. 4
    Sonstigeto separate
  5. 5
    workup.STIRRINGThe organic layer is stirred
  6. 6
    workup.ADDITION10% (w/v) aq. NaOH (4.4 vol) is added
  7. 7
    workup.STIRRINGAfter stirring for 15 to 20 minutes
  8. 8
    Sonstigeto separate
  9. 9
    TrocknenThe organic phase is then dried (Na2SO4)
  10. 10
    Filtrationfiltered
  11. 11
    Einengenconcentrated

Vorschrift

(2,2-difluoro-1,3-benzodioxol-5-yl)-methanol (1.0 eq) is dissolved in MTBE (5 vol). A catalytic amount of DMAP (1 mol %) is added and SOCl2 (1.2 eq) is added via addition funnel. The SOCl2 is added at a rate to maintain the temperature in the reactor at 15-25° C. The temperature is increased to 30° C. for 1 hour then cooled to 20° C. then water (4 vol) is added via addition funnel maintaining the temperature at less than 30° C. After stirring for an additional 30 minutes, the layers are allowed to separate. The organic layer is stirred and 10% (w/v) aq. NaOH (4.4 vol) is added. After stirring for 15 to 20 minutes, the layers are allowed to separate. The organic phase is then dried (Na2SO4), filtered, and concentrated to afford crude 5-chloromethyl-2,2-difluoro-1,3-benzodioxole that is used directly in the next step.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434717B2uspto-grants-2016_09