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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(p-Hydroxyphenyl)imidazoleHCID 82315—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-[4-(1H-imidazol-1-yl)phenoxy]ethanolHCID 1008162250%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192785
Source datasetuspto-grants-1993_03
ORD IDord-306cb22a042941c8b7a4015e8e2a4c60
Source noteuspto-grants-1993_03