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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233014Generated: October 29, 2026

Ethanolamine → 2-(2-Aminoethoxy)pyridine

https://huagongshe.com/reaction/2233014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant2-ChloropyridineHCID 7977—
ReactantSodium hydrideHCID 24758—
Solvent1,4-DioxaneHCID 31275—
Product2-(2-Aminoethoxy)pyridineHCID 96890—

Reaction Steps

A mixture of 500 mg of 2-aminoethanol and 328 mg of 60% sodium hydride-mineral oil dispersion in dioxane (27 mL) was heated to reflux for 30 min. After cooling to room temperature, 930 mg of 2-chloropyridine was added and the mixture was warmed to reflux and maintained at this temperature for 18 hrs. The reaction mixture was concentrated, diluted with water, and extracted with chloroform (3×). The organic extracts were washed with saturated brine, dried over sodium sulfate, filtered, concentrated, and the residue was purified by silica gel chromatography to give the title product as a yellow oily material. MS (M+H)+=138.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709473B2
Source datasetuspto-grants-2010_05
ORD IDord-8ac44687f63a4fd490a9183189096c5e
Source noteuspto-grants-2010_05