Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | HCID 12571560 | HCID 12571560 | — |
| Reactant | HCID 57105133 | HCID 57105133 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 67915257 | HCID 67915257 | — |
Reaction Steps
0.50 gram (0.0027 mol) of 1,3-dimethyl-4-(acetylamino)-imidazoline-2-thione (prepared by acetylating by conventional means the 1,3-dimethyl-4-amino-4-imidazoline-2-thione described in Example V) and 0.28 gram (0.003 mol) of chloroacetone were mixed together and refluxed for two hours after which time a solution 0.428 gram of sodium iodide in 5 milliliters of acetone was added whereupon a reaction took place with the immediate formation of a precipitate of sodium chloride by-product. The latter was removed by filtration and the filtrate evaporated to dryness to obtain a residue. The residue was dissolved in acetone and from the solution was recovered a solid which after purification on a Dowex-1 (Cl-) column and crystallization from isopropyl alcohol was obtained the desired 1,3-dimethyl-4-(acetylamino)-2[(2-oxopropyl)-thio]-1H-imidazolium chloride, m.p. 171°-173° 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-2e823aed3d5f47a6960cdc8cc41d770f |
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| Source note | uspto-grants-1992_03 |
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