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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1443568생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(2,2,3,3,4,4,5,5-Octafluoropentyl)-2-(3,3,4,4,4-pentafluorobutyl)malononitrile

https://huagongshe.com/reaction/1443568

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물1,1,1,2,2-Pentafluoro-4-iodobutaneHCID 110092—
반응물(2,2,3,3,4,4,5,5-Octafluoropentyl)propanedinitrileHCID 25242027—
용매Dimethyl SulfoxideHCID 679—
생성물2-(2,2,3,3,4,4,5,5-Octafluoropentyl)-2-(3,3,4,4,4-pentafluorobutyl)malononitrileHCID 2474462921.1%

반응 단계

1.4 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)malononitrile and 1.4 g of 1-iodo-3,3,4,4,4-pentafluorobutane were dissolved in 5 ml of dimethyl sulfoxide, 0.83 g of potassium carbonate was added, and the mixture was stirred at room temperature for 7 hours. Thereafter, dilute hydrochloric acid was added to the reaction mixture, followed by extraction with methyl tert-butyl ether. The organic layer was washed successively with water, aqueous saturated sodium hydrogen carbonate and aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 0.45 g of 2-(2,2,3,3,4,4,5,5-octafluoropentyl)-2-(3,3,4,4,4-pentafluorobutyl)malononitrile (hereinafter, referred to as the present compound (68)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07662402B2
출처 데이터셋uspto-grants-2010_02
ORD IDord-75c58c1092dc4dc88f8b77b557dea6c4
출처 메모uspto-grants-2010_02