반응 #3783

ord-83441b5019214471922280f5515c2e22

반응 방정식

O=C(O)Cc1c(F)cccc1Cl
2-chloro-6-fluorophenyl acetic acid
COc1cc(O)cc(OC)c1
3,5-dimethoxyphenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
COc1cc(OC)cc(Oc2cccc(F)c2CC(=O)O)c1
2-(3,5-dimethoxyphenoxy)-6-fluorophenyl acetic acid
수율 86.1%

반응 조건

온도
120°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resulting reaction solution
  2. 2
    기타was partitioned with ethyl acetate and dilute hydrochloric acid
  3. 3
    세척the organic phase was washed in water and in a saturated sodium chloride solution
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONto distill off the solvents under reduced pressure
  6. 6
    기타The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3)

실험 절차

N,N-Dimethylformamide (20 ml) was added to 2-chloro-6-fluorophenyl acetic acid (3.77 g), 3,5-dimethoxyphenol (3.08 g), potassium carbonate (5.52 g), copper iodide (950 mg) and copper (250 mg), for stirring at 120° C. for 20 hours. The resulting reaction solution was partitioned with ethyl acetate and dilute hydrochloric acid, and the organic phase was washed in water and in a saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, to distill off the solvents under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3), to recover 2-(3,5-dimethoxyphenoxy)-6-fluorophenyl acetic acid (5.27 g; yield of 86%). By 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05734067uspto-grants-1998_03