تفاعل #1447100

ord-e21fe3cf2f8d43e1b161a10802d46379

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONcharged with a stir bar
  2. 2
    أخرىmaintains below 10° C
  3. 3
    workup.STIRRINGthe resulting mixture is stirred overnight at 100° C
  4. 4
    workup.STIRRINGthe mixture is stirred for another h at 100° C
  5. 5
    أخرىThe methanol fraction is evaporated
  6. 6
    workup.ADDITIONwater (200 mL) is added to the residue
  7. 7
    استخلاصthe resulting mixture is extracted with ethyl acetate
  8. 8
    غسيلThe combined organic extracts are washed twice with water, twice with brine
  9. 9
    تجفيفdried (MgSO4)
  10. 10
    أخرىThe solvent is evaporated
  11. 11
    غسيلthe residue is washed with methanol
  12. 12
    أخرىThe insoluble residue is separated by filtration
  13. 13
    أخرىdried
  14. 14
    أخرىto give the white product

الإجراء التجريبي

KOtBu (11.8 g) is added to a flask charged with a stir bar and dry NMP (40 mL) and chilled to −10° C. under argon atmosphere. A solution of ethyl (4-ethyl-phenyl)-acetate (10.1 g) and 1-bromo-4-cyano-3,5-difluoro-benzene (11.5 g) in NMP (40 mL) is added at such a rate that the reaction temperature maintains below 10° C. After stirring for 1 hour at room temperature, methanol (50 mL) and 1 M aqueous sodium hydroxide solution (39 mL) are added and the resulting mixture is stirred overnight at 100° C. Then, 4 M aqueous hydrochloric acid (100 mL) is added and the mixture is stirred for another h at 100° C. The methanol fraction is evaporated, water (200 mL) is added to the residue and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are washed twice with water, twice with brine and dried (MgSO4). The solvent is evaporated and the residue is washed with methanol. The insoluble residue is separated by filtration and dried to give the white product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07879806B2uspto-grants-2011_02