تفاعل #1447101

ord-33c3a6ca76ba4da5871d59e2772b397e

معادلة التفاعل

CCOC(=O)Cc1ccc(CC)cc1
ethyl (4-ethyl-phenyl)-acetate
N#Cc1c(F)cc(Br)cc1F
1-bromo-4-cyano-3,5-difluoro-benzene
Cl
hydrochloric acid
CC(C)(C)[O-].[K+]
KOtBu
CCc1ccc(Cc2cc(Br)cc(F)c2C#N)cc1
1-Bromo-4-cyano-3-fluoro-5-(4-ethyl-benzyl)-benzene

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONcharged with a stir bar
  2. 2
    أخرىmaintains below 10° C
  3. 3
    استخلاصextracted with ethyl acetate
  4. 4
    تجفيفThe combined extracts are dried (Na2SO4)
  5. 5
    أخرىthe solvent is evaporated
  6. 6
    workup.DISSOLUTIONThe residue is dissolved in THF (20 mL)
  7. 7
    workup.ADDITIONtreated with 1M aqueous NaOH solution (80 mL)
  8. 8
    workup.STIRRINGAfter stirring overnight at room temperature
  9. 9
    استخلاصextracted with ethyl acetate
  10. 10
    تجفيفdried (Na2SO4)
  11. 11
    أخرىthe solvent is evaporated
  12. 12
    workup.DISSOLUTIONThe residue is dissolved in DMF (25 mL)
  13. 13
    workup.ADDITIONK2CO3 (5.5 g) is added
  14. 14
    workup.STIRRINGThe resulting mixture is stirred at 100° C. for 1 h
  15. 15
    درجة الحرارةAfter cooling to room temperature
  16. 16
    استخلاصthe resultant mixture is extracted with ethyl acetate
  17. 17
    تجفيفThe combined organic extracts are dried (MgSO4)
  18. 18
    أخرىthe solvent is evaporated
  19. 19
    أخرىThe residue is purified by chromatography on silica gel (cyclohexane/ethyl acetate 1:0->1:1)

الإجراء التجريبي

KOtBu (6.7 g) is added to a flask charged with a stir bar and dry NMP (30 mL) and chilled to −10° C. under argon atmosphere. A solution of ethyl (4-ethyl-phenyl)-acetate (5.6 g) and 1-bromo-4-cyano-3,5-difluoro-benzene (6.4 g) in NMP (20 mL) is added at such a rate that the solution temperature maintains below 10° C. After stirring for 1 hour at 10° C., the solution is neutralized with 1 M aqueous hydrochloric acid and extracted with ethyl acetate. The combined extracts are dried (Na2SO4) and the solvent is evaporated. The residue is dissolved in THF (20 mL) and treated with 1M aqueous NaOH solution (80 mL). After stirring overnight at room temperature, the solution is acidified with 4 M HCl solution and extracted with ethyl acetate. The organic extracts are combined and dried (Na2SO4) and the solvent is evaporated. The residue is dissolved in DMF (25 mL) and K2CO3 (5.5 g) is added. The resulting mixture is stirred at 100° C. for 1 h. After cooling to room temperature, the mixture is neutralized with 1 M aqueous hydrochloric acid and the resultant mixture is extracted with ethyl acetate. The combined organic extracts are dried (MgSO4) and the solvent is evaporated. The residue is purified by chromatography on silica gel (cyclohexane/ethyl acetate 1:0->1:1).

المصدر

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