반응 #1925199

ord-90e01663831d40568edc0c1eca4743a4

반응 방정식

FC(F)(F)Oc1cc(Br)ccc1I
4-bromo-2-(trifluoromethoxy)iodobenzene
CC(C)(O)C#Cc1ccc(OCCO)cc1
2-[4-(3-methyl-3-hydroxybutyne-1-yl)phenoxy]ethanol
OCCOc1ccc(C#Cc2ccc(Br)cc2OC(F)(F)F)cc1
2-(4-{2-[4-bromo-2-(trifluoromethoxy)phenyl]ethynyl}phenoxy)ethanol
수율 82.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A flask equipped with a stirrer
  2. 2
    온도under reflux for 6 hours
  3. 3
    여과After the insolubles were filtered off
  4. 4
    workup.DISTILLATIONthe solvent was distilled off
  5. 5
    workup.ADDITIONethyl acetate was added to the resulting distillate, and the pH
  6. 6
    추출ethyl acetate extraction
  7. 7
    추출The resulting extract
  8. 8
    세척was washed with NaCl saturated water
  9. 9
    건조dried over anhydrous sodium sulfate
  10. 10
    여과filtered
  11. 11
    농축concentrated
  12. 12
    기타to thereby obtain 3.85 g of a crude product in the form of a yellowish brown solid
  13. 13
    기타The crude product was then purified by silica gel column chromatography

실험 절차

A flask equipped with a stirrer and a thermometer was charged with 3.35 g (9.13 mmol) of 4-bromo-2-(trifluoromethoxy)iodobenzene and 19 ml of triethylamine under a nitrogen atmosphere. Then 1.48 g (9.13 mmol) of 2-[4-(3-methyl-3-hydroxybutyne-1-yl)phenoxy]ethanol, 13.7 mg (0.072 mmol) of copper (I) iodide, 63.2 mg (0.24 mmol) of triphenylphosphine, and 13.7 mg (0.020 mmol) of dichlorobis(triphenylphosphine)palladium were added at room temperature, and stirred under reflux for 6 hours. After the insolubles were filtered off and the solvent was distilled off, ethyl acetate was added to the resulting distillate, and the pH was adjusted to an acidity with 1N hydrochloric acid to effect ethyl acetate extraction. The resulting extract was washed with NaCl saturated water, dried over anhydrous sodium sulfate, filtered, and concentrated to thereby obtain 3.85 g of a crude product in the form of a yellowish brown solid. The crude product was then purified by silica gel column chromatography using hexane/ethyl acetate as an eluting solvent to obtain 3.0 g of 2-(4-{2-[4-bromo-2-(trifluoromethoxy)phenyl]ethynyl}phenoxy)ethanol in the form of a light yellow solid in a 82% yield.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06673267B2uspto-grants-2004_01