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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660775Generated: October 31, 2026

2-Chloroethanol → 2-(Pyridin-3-yloxy)ethan-1-ol

https://huagongshe.com/reaction/1660775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product2-(Pyridin-3-yloxy)ethan-1-olHCID 21908997—

Reaction Steps

The yield of the title compound according to D1, starting from 3-hydroxypyridine, 2-chloroethanol and K2CO3 in DMF was 19%. The title compound has also been prepared according to EP 0 286 242 A2 starting from methyl [(3-pyridinyl)oxy]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030316B2
Source datasetuspto-grants-2011_10
ORD IDord-e41a3cfeef3b472b8e3bdddc0c1a90a5
Source noteuspto-grants-2011_10