Реакция #1994254
ord-037edaeb5985468187d567d764355c27
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеThe resulting reaction mixture
- 2Температураto warm to 0° C.
- 3workup.STIRRINGto stir until the reaction mixture
- 4workup.WAITAfter this period
- 5Температураthe reaction mixture was cooled to −78° C.
- 6Температураto warm to 23° C. for 1 h
- 7ДругоеThe reaction was quenched by slow addition of saturated aqueous NH4Cl (120 mL)
- 8ЭкстракцияThe aqueous layer was thoroughly extracted with ethyl acetate (2×300 mL)
- 9СушкаThe combined organic layers were dried over anhydrous Na2SO4
- 10Фильтрацияfiltered
- 11Концентрированиеconcentrated under reduced pressure
- 12workup.DISTILLATIONThe residue was distilled under vacuum (0.12 torr) at 95° C.
Методика
Anhydrous CuCN (4.86 g, 54 mmol) was added to a solution of butadiene monooxide (38 g, 540 mmol) in anhydrous tetrahydrofuran (1.2 L) and the resulting mixture was stirred at −78° C. Commercial phenyl magnesium bromide solution (Aldrich) in ether (65 mmol) was added dropwise over a period of 10 min. The resulting reaction mixture was then allowed to warm to 0° C. and it was continued to stir until the reaction mixture was homogeneous. After this period, the reaction mixture was cooled to −78° C. and 0.58 mole of phenylmagnesium bromide solution in ether was added dropwise for 30 min. The reaction mixture was allowed to warm to 23° C. for 1 h. The reaction was quenched by slow addition of saturated aqueous NH4Cl (120 mL) followed by NH4OH (70 mL), saturated NH4Cl (500 mL) and then H2O (300 mL). The aqueous layer was thoroughly extracted with ethyl acetate (2×300 mL). The combined organic layers were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was distilled under vacuum (0.12 torr) at 95° C. to give trans-4-phenyl-2-butene-1-ol (75.6 g).