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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384592Generated: October 30, 2026

2-(Methylamino)ethanol → 2-(N-(2,6-dimethyl-4-pyridyl)-N-methylamino)ethanol

https://huagongshe.com/reaction/1384592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Methylamino)ethanolHCID 8016—
Reactant4-Chloro-2,6-dimethylpyridineHCID 588175—
CatalystHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product2-(N-(2,6-dimethyl-4-pyridyl)-N-methylamino)ethanolHCID 2262507390%

Reaction Steps

A solution of 4-chloro-2,6-dimethylpyridine (849 mg, 6 mmol), (J. Het. Chem. 1990, 1841), in 2-(methylamino)ethanol (1.35 g, 18 mmol) and 3M ethereal hydrogen chloride (3 drops) was heated at 140° C. for 1 hour. The reaction mixture was allowed to cool and was diluted with water. The insolubles were removed by filtration and the aqueous filtrate was poured onto a suspension of magnesium sulphate (50 g) in ethyl acetate (100 ml). The insolubles were removed by filtration and the filtrate dried (MgSO4) and the solvent removed by evaporation. The solid residue was triturated with ether, collected by filtration and dried under vacuum at 50° C. to give 2-(N-(2,6-dimethyl-4-pyridyl)-N-methylamino)ethanol (960 mg, 90%). m.p. 139-144° C. 1H NMR Spectrum: (CDCl3) 2.4(s, 6H); 3.0(s, 3H); 3.51(t, 2H); 3.81(t, 2H); 6.26(s, 2H) MS-ESI: 181 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258951B1
Source datasetuspto-grants-2001_07
ORD IDord-b4d3e26ece064070b889e303009f23a4
Source noteuspto-grants-2001_07