Réaction #48110

ord-912e420520564572abf02fde032e2b08

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGthe mixture is stirred overnight at room temperature
  2. 2
    AutreThe methanol fraction is evaporated
  3. 3
    Extractionextracted with tert butyl-methyl ether
  4. 4
    Extractionextracted with ethyl acetate several times
  5. 5
    AutreThe combined ethyl acetate extracts are evaporated
  6. 6
    Températurethe residue together with 120 mL of N,N-dimethyl formamide and 24.9 g of potassium carbonate heated at 100° C. for 1 hour
  7. 7
    workup.ADDITIONThe reaction mixture is diluted with aqueous sodium bicarbonate
  8. 8
    Extractionextracted several times with ethyl acetate
  9. 9
    AutreThe combined extracts are evaporated
  10. 10
    Autrethe residue crystallized from methanol

Mode opératoire

A mixture of 25 g of ethyl (4-methoxy-phenyl)-acetate, 27.4 g of 1-bromo-4-cyano-3-fluoro-benzene and 20 mL of N-methyl-pyrrolidin-2-one is slowly added to 31.4 g of potassium tert butoxide in 130 mL of N-methyl-pyrrolidin-2-one keeping the temperature below 10° C. After stirring for 1 hour at room temperature, 100 mL of methanol and 137 mL of 1 M aqueous sodium hydroxide are added and the mixture is stirred overnight at room temperature. The methanol fraction is evaporated, the residue is basified with 1 M aqueous sodium hydroxide and extracted with tert butyl-methyl ether. The aqueous phase is acidified with 4 M hydrochloric acid and extracted with ethyl acetate several times. The combined ethyl acetate extracts are evaporated and the residue together with 120 mL of N,N-dimethyl formamide and 24.9 g of potassium carbonate heated at 100° C. for 1 hour. The reaction mixture is diluted with aqueous sodium bicarbonate and extracted several times with ethyl acetate. The combined extracts are evaporated and the residue crystallized from methanol.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07745414B2uspto-grants-2010_06