HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795494Generated: October 31, 2026
1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride → HCID 17938222, compound
https://huagongshe.com/reaction/1795494
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Bis(2,4,6-trimethylphenyl)imidazolium chloride | HCID 2734211 | — |
| Reactant | Sodium 4-methylbenzenesulfonate | HCID 3720192 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 17938222 | HCID 17938222 | — |
Reaction Steps
A solution of 1.5 g (4.4 mmol) of 1,3-bis(2,4,6-trimethylphenyl)imidazolium chloride (F) in 10 ml of absolute MeOH is admixed with 0.854 g (4.4 mmol) of sodium tosylate. After the sodium tosylate has dissolved completely (magnetic stirring), the solution is evaporated under reduced pressure to a volume of about 3 ml, after which 50 ml of acetone are added. The mixture is stirred at 40° C. for two hours, the precipitated sodium chloride is filtered off and the solution is evaporated under reduced pressure to about 10 ml. After 24 hours, the white crystals which have precipitated are filtered off and washed with 5 ml of acetone and dried under reduced pressure. The yield is 1.9 g (90%). M=476.63 g/mol. This method of double decomposition can be used to replace the chloride anion by various other anions, for example carboxylate anions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026523B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-a0fe60073195417c94def38a354316b9 |
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| Source note | uspto-grants-2006_04 |
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