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HRID 394430作成日:2026年10月23日

Acetone → 2-Oxo-3,3-dimethylbutyl-thiacyclopentanium trifluoromethanesulfonate

https://huagongshe.com/ja/reaction/394430

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Diethyl EtherHCID 3283—
反応物1-(3,3-Dimethyl-2-oxobutyl)thiolan-1-ium bromideHCID 22564578—
反応物Potassium TrifluoromethanesulfonateHCID 23664779—
溶媒AcetonitrileHCID 6342—
生成物2-Oxo-3,3-dimethylbutyl-thiacyclopentanium trifluoromethanesulfonateHCID 1817594087.8%

反応手順

In a 300 ml three-necked flask, 2 g of 2-oxo-3,3-dimethylbutyl-thiacyclopentanium bromide obtained in Example 1 was dissolved in 20 ml of acetonitrile. To the solution, a solution prepared by dissolving 1.69 g of a potassium trifluoromethanesulfonate salt in 50 ml of acetonitrile was added dropwise. After stirring for three hours, the deposited potassium bromide was removed by filtration and acetonitrile was distilled off under reduced pressure by an evaporator. The residue was dissolved in chloroform and the insoluble matter was removed by filtration. Chloroform in the filtrate was distilled off under reduced pressure to obtain a transparent viscous liquid. To the transparent viscous liquid, 5 ml of acetone was added and the solution was added dropwise to 300 ml of diethyl ether. The deposited white crystal was collected by filtration and then recrystallized from ethyl acetate. The resulting white powder was dried under reduced pressure at 30° C. for six hours to obtain 2.21 g of 2-oxo-3,3-dimethylbutyl-thiacyclopentanium trifluoromethanesulfonate (yield: 87.7%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06602647B2
出典データセットuspto-grants-2003_08
ORD IDord-95bef059a97f4998bf22597655fbac5c
出典メモuspto-grants-2003_08