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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194512Generated: October 31, 2026

[2-(Methylamino)pyridin-3-yl]methanol → 2-(methylamino)nicotinaldehyde

https://huagongshe.com/reaction/2194512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(Methylamino)pyridin-3-yl]methanolHCID 4738518—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product2-(methylamino)nicotinaldehydeHCID 314935296.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

9.10 g (66.0 mmol) of (2-(methylamino)-3-pyridinyl)methanol was dissolved in chloroform (70 mL), and 17.4 g (200 mmol) of manganese dioxide was added thereto. The mixture was stirred overnight at 60° C. The reaction mixture was filtered, and the filtrate was concentrated. Thus, 8.66 g (yield: 96%) of the title compound was obtained as an orange-colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334236B2
Source datasetuspto-grants-2012_12
ORD IDord-18b9f9a658494078bf6566929d8cdac0
Source noteuspto-grants-2012_12