HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613437Generated: October 26, 2026
2-Chloroethanol → 2-[4-(1H-imidazol-1-yl)phenoxy]ethanol
https://huagongshe.com/reaction/1613437
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(p-Hydroxyphenyl)imidazole | HCID 82315 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 2-[4-(1H-imidazol-1-yl)phenoxy]ethanol | HCID 10081622 | 50% |
Reaction Steps
A stirred mixture of 8.0 g (0.050 mole) of 4(1H-imidazol-1-yl)phenol, 13.5 ml (0.20 mole) of 2-chloroethanol and 28 g (0.2 mole) of potassium carbonate in 200 ml of methyl ethyl ketone was heated at reflux, filtered, and concentrated to obtain 5.1 g of 2-[4-(1H-imidazol-1-yl)phenoxy]ethanol (50%). This alcohol (0.25 mole) and 5.2 g (0.030 mole) of sulfamic acid phenyl ester (Example 33) in 100 ml of dioxane was heated at reflux for 20 minutes, concentrated and the residual solid triturated in acetone. The triturant was acidified with an anhydrous solution of hydrogen chloride in isopropyl alcohol and the solid hydrochloride collected by filtration. The product was recrystallized from isopropyl alcohol-isopropyl ether to yield 4.26 g of solid, monohydrochloride, mp 156°-157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05192785 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-306cb22a042941c8b7a4015e8e2a4c60 |
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| Source note | uspto-grants-1993_03 |
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