反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution (50 mL) of 1-(3,5-difluoro-2-hydroxyphenyl)ethanone (2.8 g) in N,N-dimethylformamide were added potassium carbonate (6.7 g) and 2-bromo-1-cyclohexylethanone (4.0 g) synthesized in Example A51(1) at room temperature, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was allowed to cool to room temperature, and filtered through celite. Water was added to the filtrate, and the mixture was extracted with diethyl ether. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was dissolved in N,N-dimethylformamide (50 mL) again, 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 mL) was added to the solution, and the mixture was stirred at 110° C. 1 hr with heating. After cooling to room temperature, the reaction mixture was quenched with 1N hydrochloric acid, and the reaction mixture was extracted with diethyl ether. The extract was concentrated under reduced pressure, and the precipitated compound was recrystallized from diisopropyl ether-hexane to give the title object compound (3.1 g, 70%) as a colorless solid.
WORKUP
后处理
- customsynthesized in Example A51(1) at room temperature
- temperatureto cool to room temperature
- filtrationfiltered through celite
- additionWater was added to the filtrate
- extractionthe mixture was extracted with diethyl ether
- washThe extract was washed with saturated brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- dissolutionThe obtained residue was dissolved in N,N-dimethylformamide (50 mL) again
- addition1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 mL) was added to the solution
- stirringthe mixture was stirred at 110° C
- temperature1 hr with heating
- temperatureAfter cooling to room temperature
- customthe reaction mixture was quenched with 1N hydrochloric acid
- extractionthe reaction mixture was extracted with diethyl ether
- concentrationThe extract was concentrated under reduced pressure
- customthe precipitated compound was recrystallized from diisopropyl ether-hexane