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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1907085생성일: 2026년 10월 27일

Tetramethylene sulfoxide → 4-(2,2,2-Trifluoroethoxy)-1-naphthyl-tetrahydrothiophenium 2-benzoyloxy-1,1,3,3,3-pentafluoro-propane-1-sulfonate

https://huagongshe.com/reaction/1907085

반응식

참여 물질

역할이름HCID투입량
반응물Tetramethylene sulfoxideHCID 1128—
반응물Diisopropyl EtherHCID 7914—
반응물1-(2,2,2-Trifluoroethoxy)naphthaleneHCID 13443056—
반응물Sodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropanesulfonateHCID 58112889—
용매WaterHCID 962—
용매Phosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
생성물4-(2,2,2-Trifluoroethoxy)-1-naphthyl-tetrahydrothiophenium 2-benzoyloxy-1,1,3,3,3-pentafluoro-propane-1-sulfonateHCID 8666429787%

반응 단계

In 6 g of Eaton's reagent (Aldrich, diphosphorus pentoxide/methanesulfonic acid solution) was dispersed 2.4 g (0.0107 mol) of 1-(2,2,2-trifluoroethoxy)naphthalene in Synthesis Example 1-3. With stirring, 2.2 g (0.0214 mol) of tetramethylene sulfoxide was added dropwise to the dispersion. The solution was matured overnight at room temperature and combined with 30 g of water and 30 g of diisopropyl ether, from which a water layer was separated. The water layer was again washed with 30 g of diisopropyl ether. This aqueous solution was combined with 3.4 g (0.0095 mol) of sodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropanesulfonate synthesized in accordance with the teaching of JP-A 2007-145797, after which extraction was effected twice with 50 g of dichloromethane. The organic layer was washed with water and distilled in vacuum to remove the solvent. The residue was poured into isopropyl ether for crystallization, filtered and dried, obtaining the target compound. White crystals, 5.3 g, yield 87%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08597869B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-0e40b955ab584c718cf2f0d8aaaec49c
출처 메모uspto-grants-2013_12