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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50411생성일: 2026년 10월 24일

Carbon tetrafluoride → Perfluoro 4,4-dimethyl-3-isopropyl-2-pentene

https://huagongshe.com/ko/reaction/50411

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrafluorideHCID 6393—
반응물1,1,1,4,5,5,5-Heptafluoro-3-(pentafluoroethyl)-2,4-bis(trifluoromethyl)pent-2-eneHCID 121670—
반응물Potassium FluorideHCID 522689—
반응물(Trifluoromethyl)trimethylsilaneHCID 552549—
반응물1,1,1,5,5,5-Hexafluoro-3-[1-(trifluoromethyl)-1,2,2,2-tetrafluoroethyl]-2,4,4-tris(trifluoromethyl)-2-penteneHCID 22642015—
용매DimethylformamideHCID 6228—
생성물Perfluoro 4,4-dimethyl-3-isopropyl-2-penteneHCID 73990785—

반응 단계

1 mmol (450 mg) of perfluoro(3-ethyl-2,4-dimethyl-2-pentene) and 4.0 mmol (568.8 mg) of trifluoromethyltrimethylsilane were weighed into a 10-ml fluororesin-made reaction container, then 1 ml of dimethyl formamide and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added therein. A fluororesin-made magnetic stirrer was placed and the mixture was stirred vigorously for 1 hour at room temperature, and then 1.0 mmol of trifluoromethyltrimethylsilane (142.2 mg) and 0.1 mmol of acidic potassium fluoride (KHF2, 7.8 mg) were added and the mixture was further stirred vigorously for 1 hour at room temperature. After completion of the reaction, the transparent lower perfluorocarbon layer was analyzed by gas chromatography using a capillary column (NB-1, 0.25 μm, 1.5 mm ID×60 m). The yield of the main product perfluoro(2,4,4-trimethyl-3-isopropyl-2-pentene) was 74.5% by weight. As the by-product, perfluoro 4,4-dimethyl-3-isopropyl-2-pentene was obtained at the yield of 25.5% by weight. The starting material perfluoro(3-ethyl-2,4-dimethyl-2-pentene) was consumed completely by the reaction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710214B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-13ce255a86bf4c28b9543ff9474bc153
출처 메모uspto-grants-2004_03