돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394428생성일: 2026년 10월 24일

Potassium Trifluoromethanesulfonate → 2-Oxobutyl-thiacyclopentanium trifluoromethanesulfonate

https://huagongshe.com/ko/reaction/394428

반응식

참여 물질

역할이름HCID투입량
반응물Potassium TrifluoromethanesulfonateHCID 23664779—
반응물2-Oxobutyl-thiacyclohexanium bromideHCID 85787952—
용매AcetonitrileHCID 6342—
생성물2-Oxobutyl-thiacyclopentanium trifluoromethanesulfonateHCID 8658489069.8%

반응 조건

온도-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602647B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-1292fc0bf1b9431fa40cdfb82ef84c80
출처 메모uspto-grants-2003_08