Реакция #2186184
ord-7d7c046e958449359da2eea064547cb2
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеThe resulting reaction mixture
- 2workup.WAITthe mixture was left at rest
- 3Другоеto separate into an organic layer
- 4Экстракцияby extracting to the organic layer
- 5ПромывкаThe resulting organic layer was washed with a sodium chloride aqueous solution in three times
- 6Сушкаdried over anhydrous magnesium sulfate
- 7Концентрированиеconcentrated under reduced pressure
- 8Другоеto obtain a residue
- 9Другое19.7 g of the residue was purified by recrystallization from a mixed solvent of heptane and toluene (heptane/toluene=2/1 by volume)
Методика
22.0 g of the compound (b66) was dissolved in 200 mL of methylene chloride. 23.7 g of boron tribromide was added dropwise to the resulting solution in a temperature range of −27 to −20° C., and the temperature of the solution was gradually increased to room temperature, followed by stirring overnight. The resulting reaction mixture was poured slowly to 300 mL of iced water, and the mixture was left at rest to separate into an organic layer and an aqueous layer, followed by extracting to the organic layer. The resulting organic layer was washed with a sodium chloride aqueous solution in three times, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain a residue. The residue was a yellowish solid. 19.7 g of the residue was purified by recrystallization from a mixed solvent of heptane and toluene (heptane/toluene=2/1 by volume) to obtain 18.0 g of 3-chloro-2-fluoro-4′-propylbiphenyl-4-ol (b67). The resulting compound (b67) was a white solid.