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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405012생성일: 2026년 10월 24일

Water → HCID 86632756, 화합물

https://huagongshe.com/ko/reaction/405012

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Triphenylsulfonium chlorideHCID 61343—
반응물HCID 86650905HCID 86650905—
용매ChloroformHCID 6212—
생성물HCID 86632756HCID 8663275697%

반응 단계

A 2 L reactor was charged with 183.7 g (38% purity, 0.38 mole) of sodium 2-hydroxy-1,1-difluoroethanesulfonic acid, 300 mL of water, 450 mL of chloroform and an aqueous solution of triphenylsulfonium chloride [142.8 g (0.49 mole/1.25 equivalents) of triphenylsulfonium chloride and 150 mL of water], followed by stirring at room temperature for 1 hour. A reaction solution was analyzed by using nuclear magnetic resonance (NMR), by which there was found almost half the raw material sodium 2-hydroxy-1,1-difluoroethanesulfonic acid remaining. Accordingly, the reactor was further charged with the aqueous solution of triphenylsulfonium chloride [142.8 g (0.49 mole/1.25 equivalents) of triphenylsulfonium chloride and 150 mL of water], followed by stirring at room temperature for 0.5 hour (triphenylsulfonium chloride was used in an amount of 285.7 g (0.96 mole/2.5 equivalents) in total and the reaction time was 1.5 hours in total). The reaction solution was analyzed by using nuclear magnetic resonance (NMR), by which the raw material was detected being consumed. Thereafter, the reaction solution was separated. The obtained water layer was extracted with 100 mL of chloroform three times while distilling a solvent out of the obtained organic layer, thereby obtaining 328.2 g of the target triphenylsulfonium 2-hydroxy-1,1-difluoroethanesulfonate. In this case, the purity was 48% and the yield was 97%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748672B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-7d525ea3ae0e4186b6f58d6de61ff2e1
출처 메모uspto-grants-2014_06