Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl triflate | HCID 9526 | — |
| Reactant | HCID 15165836 | HCID 15165836 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67915249 | HCID 67915249 | — |
Reaction Steps
To a solution of 0.25 gram (0.001 mol) of the 1-methyl-5-phenyl-2[(2-oxopropyl)thio]imidazole, prepared as above described, in 10 mL of methylene chloride was added 0.164 g (0.001 mol) of methyl trifluoromethanesulfonate, and the solution was stirred overnight at room temperature. The solvent was evaporated and the residue was converted to the chloride ion form by dissolving in 20% methanol/water and passing through Dowex-1 (Cl-)ion exchange column. The column was eluted with 20 percent methanol in water and the eluate subjected to reduced pressure to evaporate the solvent and to obtain a residue. The residue was stirred overnight in ethyl acetate, filtered and recrystallized from isopropanol/hexane to obtain purified 1,3-dimethyl 4-phenyl-2[(2-oxopropyl)thio]-1H-imidazolium chloride, m.p. 143°-146° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098707 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-7aa2f9bb7f8d431daae7cccba8ded60f |
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| Source note | uspto-grants-1992_03 |
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