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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737635Generated: October 31, 2026

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

https://huagongshe.com/reaction/1737635

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 numberUS05962458
Source datasetuspto-grants-1999_10
ORD IDord-16dd58bf06ba4a15a3d44e7fb8cffe31
Source noteuspto-grants-1999_10