HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439604Generated: October 28, 2026
Ethanol → (5-Chloro-2-ethyl-1h-imidazol-4-yl)methanol
https://huagongshe.com/reaction/439604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Trichloroisocyanuric Acid | HCID 6909 | — |
| Reactant | Ethyl-4,5-bis(hydroxymethyl) imidazole | HCID 13608920 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (5-Chloro-2-ethyl-1h-imidazol-4-yl)methanol | HCID 10241096 | — |
Reaction Steps
1.53 Grams (6.6 mmol) of trichloroisocyanuric acid was added little by little to a solution consisting of 2.03 g (13 mmol) of the 2-ethyl-4,5-bis(hydroxymethyl) imidazole, 100 ml of ethanol and 40 ml of 1,4-dioxane at room temperature with stirring over a period of about 10 minutes. The mixture was stirred at the same temperature for one hour, the solvent was distilled off under reduced pressure, the reaction product was extracted with ethanol, and the extract was evaporated to dryness under reduced pressure. The resulting solid product was then extracted with acetone, the extract was concentrated and was then subjected to the column chromatography (silica gel-acetone), and the effluent was further concentrated and was recrystallized from acetonitrile to obtain a 2-ethyl-4-chloro-5-(hydroxymethyl) imidazole in an amount of 0.78 g (yield, 37.4%). The TLC and spectra were measured to be the same as those of Example 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514811 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-248267d671be4c5a88fcd2a14e28cc98 |
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| Source note | uspto-grants-1996_05 |
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