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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327649Generated: October 30, 2026

2-Chloroethanol → 2-(3-nitrophenoxy)ethanol

https://huagongshe.com/reaction/327649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantMethaneHCID 297—
Reactant3-NitrophenolHCID 11137—
ReactantPotassium CarbonateHCID 11430—
SolventMethanolHCID 887—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-(3-nitrophenoxy)ethanolHCID 4668927—

Reaction Steps

A mixture of m-nitrophenol (28 g, 0.2 mole), 2-chloroethanol (53.6 ml, 0.8 mole), and potassium carbonate (110.4 g, 0.8 mole) in 300 ml methyl ethyl ketone was kept at reflux temperature with stirring overnight. The solid was filtered and dissolved in water. The filtrate was concentrated and some wolid was crystallized from 2-propanol/isopropyl ether. This light-brown solid was collected and weighed 22.78 g (62%). The mother liquor was concentrated and redissolved in toluene/ethyl acetate and extracted with the above aqueous solution. The aqueous layer was further extracted with fresh toluene/ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered, and concentrated to give a second crop of 6.46 g (17.6%). The second crop was dissolved in methanol, stirred with charcoal, filtered, evaporated, and crystallized from 2-propanol/isopropyl ether to give a pure sample. The sample was dried under vacuum at room temperature overnight, mp 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273993
Source datasetuspto-grants-1993_12
ORD IDord-f9318754b4fe44c4a41e4b4dd789dcb8
Source noteuspto-grants-1993_12