참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Trifluoromethanesulfonate | HCID 23664779 | — |
| 반응물 | 2-Oxobutyl-thiacyclohexanium bromide | HCID 85787952 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Oxobutyl-thiacyclopentanium trifluoromethanesulfonate | HCID 86584890 | 69.8% |
반응 단계
In a 300 ml three-necked flask, 2 g of 2-oxobutyl-thiacyclohexanium bromide obtained in Example 1 was dissolved in 10 ml of acetonitrile. To the solution, a solution prepared by dissolving 1.6 g of a potassium trifluoromethanesulfonate salt in 100 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 and the residue (transparent viscous liquid) was cooled in a refrigerator at −20° C. for three hours. The residue was converted into a white crystal by cooling. The white crystal was recrystallized from ethyl acetate and then dried under reduced pressure at 30 ° C. for six hours to obtain 1.7 g of 2-oxobutyl-thiacyclopentanium trifluoromethanesulfonate (yield: 65.8%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06602647B2 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-1292fc0bf1b9431fa40cdfb82ef84c80 |
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| 출처 메모 | uspto-grants-2003_08 |
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