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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279673Generated: October 29, 2026

Dimethylamine → [2-(dimethylamino)-4-pyridinyl]methanol(SALTDATA: HCl)

https://huagongshe.com/reaction/279673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant(2-Chloropyridin-4-yl)methanolHCID 7062237—
SolventEthanolHCID 702—
Product[2-(dimethylamino)-4-pyridinyl]methanol(SALTDATA: HCl)HCID 2262506694%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 2-chloro-4-hydroxymethylpyridine (1.0 g, 7 mmol), (prepared as described for the starting material in Example 58), and dimethylamine (30 ml of a 30% solution in ethanol) was heated in a Carius tube for 16 hours at 200° C. The mixture was allowed to cool and the mixture partitioned between saturated aqueous sodium bicarbonate solution and ethyl acetate. The organic layer was separated, dried (MgSO4) and the volatiles removed by evaporation. The residue was purified by column chromatography eluting with ethyl acetate to give 4-hydroxymethyl-2-(dimethylamino)pyridine (1 g, 94%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362336B1
Source datasetuspto-grants-2002_03
ORD IDord-1efc2d88839847949e671cd7816de0e3
Source noteuspto-grants-2002_03