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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Trimethyl Phosphate | HCID 10541 | — |
| Reactant | 1,2,3,4-Tetramethylimidazolinium methyl carbonate | HCID 67521362 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,2,3,4-Tetramethylimidazolinium dimethyl phosphate | HCID 67521527 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08177994B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-fe0c3568818a47f0b9ce8903c4863cea |
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| Source note | uspto-grants-2012_05 |
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