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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetramethylene sulfoxide | HCID 1128 | — |
| 반응물 | Diisopropyl Ether | HCID 7914 | — |
| 반응물 | 1-(2,2,2-Trifluoroethoxy)naphthalene | HCID 13443056 | — |
| 반응물 | Sodium 2-benzoyloxy-1,1,3,3,3-pentafluoropropanesulfonate | HCID 58112889 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Phosphorus Pentoxide-Methanesulfonic Acid | HCID 86584057 | — |
| 생성물 | 4-(2,2,2-Trifluoroethoxy)-1-naphthyl-tetrahydrothiophenium 2-benzoyloxy-1,1,3,3,3-pentafluoro-propane-1-sulfonate | HCID 86664297 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08597869B2 |
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| 출처 데이터셋 | uspto-grants-2013_12 |
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| ORD ID | ord-0e40b955ab584c718cf2f0d8aaaec49c |
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| 출처 메모 | uspto-grants-2013_12 |
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