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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1873108생성일: 2026년 10월 26일

Tetrahydrofuran → Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)

https://huagongshe.com/reaction/1873108

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Diphenyl sulfoxideHCID 13679—
반응물Trimethylsilyl triflateHCID 65367—
반응물HCID 178418255HCID 178418255—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
용매Trifluoromethanesulfonic acidHCID 62406—
생성물Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 1172932050%

반응 조건

온도-78 °C

반응 단계

2.0 g of phenyl sulfoxide dissolved in 20 mL dichloromethane was cooled to -78° C. and then, 2.3 mL trimethylsilyl triflate was slowly added to the mixture for more than 5 minutes. The reacting mixture was stirred at the same temperature for 10 minutes and with the gradual increase of reaction temperature, stirred at 0° C. for 30 minutes. The solution was again cooled to -78° C. and 10 mL tetrahydrofuran solution of 2.0 M phenyl magnesium bromide was slowly added to the reacting solution. The reacting mixture was stirred at the same temperature for 30 minutes and further stirred at 0° C. for 30 minutes. The reaction was completed in 30 mL of 3% triflic acid aqueous solution. The reactant was diluted with 200 mL ether and extracted two times with 30 mL of triflic acid aqueous solution. The aqueous solution, so extracted, was further extracted three times with 30 mL chloroform. After collection of the organic layer, the solution was dried over anhydrous Na2SO4 and filtrated to remove the solvent. Thus, 1.9 g of triphenyl sulfonium triflate (yield: 50%) was obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06111143
출처 데이터셋uspto-grants-2000_08
ORD IDord-151f411783c244c3b1a19edf7fb18644
출처 메모uspto-grants-2000_08