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
An oven dried Schlenk tube equipped with a rubber septum was cooled under an argon purge. The septum was removed and the tube was charged with palladium acetate (5.6 mg, 0.025 mmol, 5 mol % Pd), (−)-2-(dicyclohexylphosphino)-2′-(dimethylamino)-1,1′-binaphthyl (10.5 mg, 0.038 mmol, 7.5 mol %) and 2-methyl-5-(N-methyl-anilinomethylene)cyclopentanone (108 mg, 0.5 mmol). Toluene (2 mL) was added and the mixture was stirred for 1 min at room temperature. 4-Bromobenzonitrile (182 mg, 1.0 mmol) and sodium t-butoxide (96 mg, 1.0 mmol) were added to the tube. The tube was capped with the septum, purged with argon, and additional toluene (4 mL) was added through the septum. The mixture was heated to 100° C. with stirring until the starting ketone had been completely consumed as judged by GC analysis. The mixture was cooled to room temperature, quenched with saturated aqueous ammonium chloride (10 mL) and diluted with ether (20 mL). The mixture was poured into a separatory funnel and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel to afford 80 mg (51%) of the title compound. The ee was determined to be 80% by chiral HPLC analysis.
WORKUP
后处理
- customAn oven dried Schlenk tube
- customequipped with a rubber septum
- temperaturewas cooled under an argon
- custompurge
- customThe septum was removed
- customThe tube was capped with the septum
- custompurged with argon, and additional toluene (4 mL)
- additionwas added through the septum
- temperatureThe mixture was heated to 100° C.
- stirringwith stirring until the starting ketone
- customhad been completely consumed
- temperatureThe mixture was cooled to room temperature
- customquenched with saturated aqueous ammonium chloride (10 mL)
- additiondiluted with ether (20 mL)
- additionThe mixture was poured into a separatory funnel
- customthe layers were separated
- extractionThe aqueous layer was extracted with ether (20 mL)
- washthe combined organic layers were washed with brine (20 mL)
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude material was purified by flash chromatography on silica gel