تفاعل #1596949
ord-6b6fca11ffde44caa23c7ed1b1b426d8
معادلة التفاعل
المتفاعلات
ظروف التفاعل
المعالجة
- 1أخرىthe organic phase is separated off
- 2غسيلThe aqueous phase is washed with MTBE
- 3غسيلthe combined organic phases are washed with saturated sodium chloride solution
- 4أخرىdried
- 5تركيزThe solution is concentrated to dryness
- 6أخرىthe crude product is purified by column chromatography (SiO2, n-heptane:toluene=1:1)
- 7أخرىThe further purification
- 8أخرىis carried out by recrystallisation from ethanol and n-heptane
الإجراء التجريبي
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.