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
0.361 g meta-chloro-perbenzoic acid were added into a solution of 0.262 g 1-(4,4-difluoro-cyclohexyl)-ethanone in 5 ml chloroform. The reaction was stirred at rt for 2 hours when TLC indicated consumption of the 1-(4,4-difluoro-cyclohexyl)-ethanone. The solution was poured into saturated sodium hydrogencarbonate solution and extracted with chloroform (3×50 ml). The combined organic phases were passed through a phase separator concentrated in vacuo. The crude product was resuspended in methanol (5 ml) and 10% aq. potassium carbonate solution. (5 ml) and stirred at rt over a weekend. The solution was diluted with chloroform (25 ml) and sat. sodium hydrogencarbonate solution. The organic phases were separated and the aqueous phase was extracted with methylene chloride (3×25 ml). The combined organic phases were passed through a phase-separator, concentrated in vacuo. Purification was achieved by silica gel column chromatography (solvent: 100%→1:1 petroleum ether/diethylether).
WORKUP
后处理
- customconsumption of the 1-(4,4-difluoro-cyclohexyl)-ethanone
- additionThe solution was poured into saturated sodium hydrogencarbonate solution
- extractionextracted with chloroform (3×50 ml)
- concentrationconcentrated in vacuo
- stirring(5 ml) and stirred at rt over a weekend
- additionThe solution was diluted with chloroform (25 ml) and sat. sodium hydrogencarbonate solution
- customThe organic phases were separated
- extractionthe aqueous phase was extracted with methylene chloride (3×25 ml)
- concentrationconcentrated in vacuo
- customPurification