HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248428Generated: October 30, 2026
Methanesulfonic Acid → HCID 13363494, compound
https://huagongshe.com/reaction/1248428
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 3023813 | HCID 3023813 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 13363494 | HCID 13363494 | — |
Reaction Steps
A mixture of 6 parts of 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)-1-propanone and 30 parts of methanesulfonic acid was stirred till all solid entered solution. After cooling, 5.5 parts of 1,2-ethanedithiol were added while nitrogen gas was introduced. The whole was stirred overnight at room temperature. The reaction mixture was diluted with trichloromethane till a volume of 150 parts. This solution was added dropwise to a vigorously stirred solution of potassium carbonate in water. The organic phase was separated, washed with water, dried, filtered and evaporated. The oily residue was converted into the nitrate salt in 2-propanol. 2,2'-Oxybispropane was added till turbid and the formed salt was allowed to crystallize. It was filtered off and dried, yielding 6 parts of 2-(2,4-dichlorophenyl)-2-[1-(1H-imidazol-1-yl)ethyl]-1,3-dithiolane; mp. 141.9° C. (compound 29).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04524110 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-6690da7c21354d16a7357b13ee1210d0 |
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| Source note | uspto-grants-1985_06 |
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