Reaktion #159954

ord-26b8b4cf5263426fbdedf8d120e736dd

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction liquid
  2. 2
    workup.ADDITIONwas added
  3. 3
    Filtrationfollowed by filtration
  4. 4
    workup.ADDITIONAdding 100 mL of water to the filtrate
  5. 5
    Sonstigethe organic layer was separated
  6. 6
    ExtraktionThe aqueous layer was extracted with 100 mL of diethyl ether
  7. 7
    Waschenwashed twice with 20 mL of water and once with 10 mL of saturated brine by the order
  8. 8
    Trocknendried over magnesium sulfate
  9. 9
    workup.DISTILLATIONDistilling the solvent off under reduced pressure

Vorschrift

A mixture of 4′-fluoro-3′-nitroacetophenone 2.04 g, ethyl 3-(1H-imidazol-2-yl)propanoate 1.87 g, potassium carbonate 3.07 g and N,N-dimethylacetamide 28 mL was heated at 100° C. for 16.5 hours. The reaction liquid was allowed to cool off and to which 60 mL of diethyl ether was added, followed by filtration. Adding 100 mL of water to the filtrate, the organic layer was separated. The aqueous layer was extracted with 100 mL of diethyl ether. The extract was combined with the organic layer, washed twice with 20 mL of water and once with 10 mL of saturated brine by the order stated, and dried over magnesium sulfate. Distilling the solvent off under reduced pressure, 2.54 g of the title compound was obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08829000B2uspto-grants-2014_09