反应详情

Compound 1 (6.3 g, 3.7 mmol, 1 equiv) and iodopentafluorobenzene (5.5 mL, 4 mmol, 1.2 equiv) were dissolved in toluene (120 mL). 1.0 M Potassium carbonate solution (120 mL), tetrabutylammonium bromide (600 mg), and tetrakis(triphenylphosphine)palladium(0) (2.1 g, 1.8 mmol, 0.05 equiv) were added. Nitrogen was sparged through the mixture for 10 minutes. The reaction was refluxed 18 hours, then cooled to room temperature. The layers were separated and the aqueous layer was extracted with methyl tert-butyl ether (2×50 mL). The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. The residue was purified over silica gel (100 g), eluting with a gradient of 0 to 4% ethyl acetate in heptane to give 2,3,4,5,5′,6-hexafluoro-2′-methoxy-1,1′-biphenyl (2) (3.0 g, 28% yield) as an off-white solid.

1. customNitrogen was sparged through the mixture for 10 minutes
2. temperatureThe reaction was refluxed 18 hours
3. customThe layers were separated
4. extractionthe aqueous layer was extracted with methyl tert-butyl ether (2×50 mL)
5. dry with materialThe combined organic layers were dried over sodium sulfate
6. concentrationconcentrated under reduced pressure
7. customThe residue was purified over silica gel (100 g)
8. washeluting with a gradient of 0 to 4% ethyl acetate in heptane