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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396601생성일: 2026년 10월 24일

Dimethyl Sulfate → Propane, 1,1,1,2,2,3,3-heptafluoro-3-methoxy-

https://huagongshe.com/ko/reaction/396601

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfateHCID 6497—
반응물DiglymeHCID 8150—
반응물Perfluoropropionyl fluorideHCID 67912—
반응물Potassium FluorideHCID 522689—
용매WaterHCID 962—
생성물Propane, 1,1,1,2,2,3,3-heptafluoro-3-methoxy-HCID 277494399.9%

반응 조건

온도-20 °C

반응 단계

A jacketed one liter round bottom flask was equipped with an overhead stirrer, a solid carbon dioxide/acetone condenser, and an addition funnel. The flask was charged with spray-dried potassium fluoride (85 g, 1.46 mol) and anhydrous diethylene glycol dimethyl ether (375 g) and was then cooled to about −20° C. using a recirculating refrigeration system. C2F5COF (196 g, 1.18 mol) was added to the flask over a period of about one hour. The flask was then warmed to about 24° C., and dimethyl sulfate (184.3 g, 1.46 mol) was then added dropwise via the addition funnel over a 45 minute period. The resulting mixture was then stirred at room temperature overnight. Water (a total of 318 mL) was then added dropwise to the mixture. The mixture was transferred to a one liter round bottom flask, and the resulting product ether was azeotropically distilled. The lower product phase of the resulting distillate was separated from the upper aqueous phase, was washed once with cold water, and was subsequently distilled to give 180 g of product (b.p. 36° C.;>99.9% purity by GLC). The product identity was confirmed by GCMS and by 1H and 19F NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608019B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-da3db3e57fb04e32aa52041059c497a1
출처 메모uspto-grants-2003_08