Réaction #1596949
ord-6b6fca11ffde44caa23c7ed1b1b426d8
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1Autrethe organic phase is separated off
- 2LavageThe aqueous phase is washed with MTBE
- 3Lavagethe combined organic phases are washed with saturated sodium chloride solution
- 4Autredried
- 5ConcentrationThe solution is concentrated to dryness
- 6Autrethe crude product is purified by column chromatography (SiO2, n-heptane:toluene=1:1)
- 7AutreThe further purification
- 8Autreis carried out by recrystallisation from ethanol and n-heptane
Mode opératoire
5.20 g (15.0 mmol) of 5-ethyl-2-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]tetrahydropyran are initially introduced in 35 ml of THF together with 6.93 g (15.0 mmol) of 5-((4-bromo-2,6-difluorophenyl)-difluoromethoxy)-1,3-difluoro-2-(trifluoromethyl)benzene. 590 mg (0.75 mmol) of bis(tri-o-tolylphosphine)palladium(II) chloride and 0.1 ml (0.75 mmol) of triethylamine are added. The mixture is heated to 50° C., and a solution of 2.41 g (24.0 mmol) of potassium hydrogencarbonate in 15 ml of water is added. After 3 h at this temperature, water and MTBE are added, and the organic phase is separated off. The aqueous phase is washed with MTBE, and the combined organic phases are washed with saturated sodium chloride solution and dried using sodium sulfate. The solution is concentrated to dryness, and the crude product is purified by column chromatography (SiO2, n-heptane:toluene=1:1). The further purification is carried out by recrystallisation from ethanol and n-heptane, giving 2-{4′-[(3,5-difluoro-4-trifluoromethylphenoxy)difluoromethyl]-2,3′,5′-trifluorobiphenyl-4-yl}-5-ethyltetrahydropyran as a colourless solid having an m.p. of 90° C.