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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171977생성일: 2026년 10월 25일

1-Methylimidazole → 1-Methyl-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)imidazolium iodide

https://huagongshe.com/reaction/1171977

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctaneHCID 74888—
용매TolueneHCID 1140—
생성물1-Methyl-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)imidazolium iodideHCID 15495093103.5%

반응 조건

온도110 °C

반응 단계

1-Methylimidazole (4.32 g, 0.52 mol) was partially dissolved in reagent-grade toluene (50 ml) in a large round-bottomed flask and stirred vigorously. 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane (26 g, 0.053 mol) was added, and the mixture was heated under reflux at 110 degrees C. for 24 hours. The solvent was removed under vacuum giving 1-methyl-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)imidazolium iodide (30.5 g) as a waxy solid. Potassium 1,1,2,2-tetrafluoroethanesulfonate (TFES-K, 12 g) was added to reagent grade acetone (100 ml) in a separate round-bottomed flask, and this solution was carefully added to the 1-methyl-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)imidazolium iodide which had been dissolved in acetone (50 ml). The reaction mixture was heated under reflux for approximately 16 hours. The reaction mixture was then filtered using a large frit glass funnel to remove the white KI precipitate formed, and the filtrate was placed on a rotary evaporator for 4 hours to remove the acetone. The oily liquid was then filtered a second time to yield the product, as shown by proton NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829706B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-7009330ca6534fab9b24492d2a1bc12f
출처 메모uspto-grants-2010_11