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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923419Generated: November 3, 2026

Water → 1,2,3,4-Tetramethylimidazolinium dimethyl phosphate

https://huagongshe.com/reaction/1923419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrimethyl PhosphateHCID 10541—
Reactant1,2,3,4-Tetramethylimidazolinium methyl carbonateHCID 67521362—
SolventMethanolHCID 887—
Product1,2,3,4-Tetramethylimidazolinium dimethyl phosphateHCID 67521527—

Reaction Conditions

Temperature100 °C

Reaction Steps

By adding trimethyl phosphate (TMP, produced by Daihachi Chemical Industries Co., Ltd.) (0.1 mol) to a methanol solution of 1,2,3,4-tetramethylimidazolinium methyl carbonate salt (0.1 mol) obtained in the same manner as Example 1, adding water (0.3 mol) and stirring the mixture at 100° C. for 20 hours, the trimethyl phosphate was hydrolyzed and, at the same time, a salt exchange reaction was performed. As a result, a methanol solution of 1,2,3,4-tetramethylimidazolinium dimethyl phosphate monoanion was obtained. The resulting solution was heated at a pressure reduction degree of 1.0 kPa or less at 50° C., so that methanol was evaporated until methanol was no longer distilled off. By increasing the temperature from 50° C. to 100° C. and heating the mixture for 30 minutes to distill by-products off, an electrolyte (c5) {1,2,3,4-tetramethylimidazolinium dimethyl phosphate monoanion} was obtained. The yield was 99 wt %. The content of dimethyl phosphoric acid monoanion in the anions was 99% by mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08177994B2
Source datasetuspto-grants-2012_05
ORD IDord-fe0c3568818a47f0b9ce8903c4863cea
Source noteuspto-grants-2012_05