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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327642Generated: October 25, 2026

2-Chloroethanol → 2-[4-(1H-1,2,4-Triazol-1-yl)phenoxy]ethanol

https://huagongshe.com/reaction/327642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(1,2,4-Triazol-1-yl)phenolHCID 110064—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-[4-(1H-1,2,4-Triazol-1-yl)phenoxy]ethanolHCID 19108673—

Reaction Steps

A stirred mixture of 4(1H-1,2,4-triazol-1-yl)phenol (16.1 g, 0.10 mole), 2-chloroethanol (25.5 g, 0.30 mole), potassium carbonate (42 g, 0.30 mole) and methyl ethyl ketone (100 ml) was heated at reflux temperature for 10 hr. An additional 16.1 g (0.20 mole) of 2-chloroethanol was added to the reaction mixture and heating at reflux temperature continued for another 24 hr. The hot mixture was filtered and the filtrate chilled. The crystalline precipitate was collected by filtration and the filter cake rinsed with water to remove most of the dark color. The solid was triturated with hot ethyl acetate, the mixture cooled, and the light tan crystals collected to yield 14.0 g (68%); mp 151°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273993
Source datasetuspto-grants-1993_12
ORD IDord-926abf54928b495c941c665097d8b65d
Source noteuspto-grants-1993_12