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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421065Generated: November 1, 2026

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

https://huagongshe.com/reaction/1421065

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 numberUS06071921
Source datasetuspto-grants-2000_06
ORD IDord-41b62a14da8a42a390203bcce65d6273
Source noteuspto-grants-2000_06