돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 640659생성일: 2026년 10월 24일

Hydrochloric Acid → 1-Butyl-3-methylimidazolium tetrafluoroborate

https://huagongshe.com/ko/reaction/640659

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Tetrafluoroboric acidHCID 28118—
반응물1,4-DioxaneHCID 31275—
반응물1,4-Dioxane--water (1/1)HCID 21886435—
반응물HCID 178448538HCID 178448538—
생성물1-Butyl-3-methylimidazolium tetrafluoroborateHCID 273417899%

반응 단계

116.5 g (0.667 mol) of 1-butyl-3-methylimidazolium chloride are initially introduced at 70° C. in the liquid state and dissolved in 120.6 g of approx. 50% aqueous HBF4 (approx. 3% excess). No warming and only slight HCl gas formation is observed in the process. 250 ml of 1,4-dioxane are subsequently added, and 250 ml of HCl-containing water/dioxane azeotrope are distilled off at atmospheric pressure (85-90° C.). A further 200 ml of dioxane are then added, and 250 ml of HCl-containing water/dioxane mixture are distilled off at atmospheric pressure (85-101° C.). The residue in the distillation flask has a low content of chloride ions (silver nitrate test). After a further azeotropic distillation with 100 ml of dioxane, the chloride ion content in the residue is too low to be detected using the silver nitrate test. Drying of the distillation residue under reduced pressure at 1.3 Pa and 80° C. gives 149.2 g of 1-butyl-3-methylimidazolium tetrafluoroborate as liquid. The yield of 1-butyl-3-methylimidazolium tetrafluoroborate is approximately quantitative. The chloride content in the ionic liquid is 11 ppm, measured by microtitration using a silver nitrate solution in non-aqueous medium. The end point is determined potentiometrically using a Cl-selective electrode.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07692007B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-6353b67dde9144a8936c0bcd6da4be0b
출처 메모uspto-grants-2010_04