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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737633Generated: October 31, 2026

Methylamine → (2-(Methylamino)pyridin-4-yl)methanol

https://huagongshe.com/reaction/1737633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant(2-Chloropyridin-4-yl)methanolHCID 7062237—
SolventEthanolHCID 702—
Product(2-(Methylamino)pyridin-4-yl)methanolHCID 2262503446%

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 methylamine (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 hydrogen carbonate 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-(methylamino)pyridine (440 mg, 46%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962458
Source datasetuspto-grants-1999_10
ORD IDord-75577af1929b4deea6143a9b1cb41cf3
Source noteuspto-grants-1999_10