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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493019Generated: October 31, 2026

1-Methylimidazole → HCID 12983283, compound

https://huagongshe.com/reaction/493019

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantHCID 131727443HCID 131727443—
SolventDichloromethaneHCID 6344—
ProductHCID 12983283HCID 12983283—

Reaction Steps

(2,2,2-Trifluoroethyl)(4-fluorophenyl)iodonium bis(trifluoromethanesulfonyl)imide (17.6 g, 30 mmol) and methylene chloride (60 ml) were placed in a reaction vessel to convert the inside of the reaction vessel to a nitrogen atmosphere. While stirring and cooling in an ice bath, 1-methylimidazole (2.46 g, 30 mmol) was added dropwise thereto. After the dropwise addition thereof, the ice bath was removed, and the mixture was allowed to react at room temperature for 3 hours. After the completion of the reaction, the solvent was removed by distillation. The resulting liquid product was washed with hexane (or pentane), water, and then hexane (or pentane). Subsequently, this liquid product was dissolved in a small amount of ethyl acetate, and a large amount of ether was added thereto to separate the liquid product. The liquid product was separated from the solvent and then dried at 110° C. for 6 hours under reduced pressure using a vacuum pump. Thus, pure 1-methyl-3-(2′,2′,2′-trifluoroethyl)imidazolium bis(trifluoromethanesulfonyl)imide (compound 9) was obtained as a liquid substance (yield 11.5 g, 86%). When the product is colored, it may be subjected to decolorization with active carbon. Separately, p-fluoroiodobenzene was obtained from the aforementioned hexane (or pentane) wash in a substantially quantitative manner.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534509B2
Source datasetuspto-grants-2009_05
ORD IDord-6390edf9a05a470fb3f5f813969be8ee
Source noteuspto-grants-2009_05