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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478723Generated: October 30, 2026

3-Hydroxymethyl-6-methyl-2-(3-nitrophenylamino)pyridine → 6-Methyl-2-(3-nitrophenylamino)nicotinaldehyde

https://huagongshe.com/reaction/478723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Hydroxymethyl-6-methyl-2-(3-nitrophenylamino)pyridineHCID 18002619—
CatalystHCID 178418406HCID 178418406—
SolventChloroformHCID 6212—
Product6-Methyl-2-(3-nitrophenylamino)nicotinaldehydeHCID 1800264672.1%

Reaction Steps

To a suspension of 3-hydroxymethyl-6-methyl-2-(3-nitrophenylamino)pyridine (11.05 g, 42.62 mmol) in chloroform (200 ml) was added manganese dioxide (50 g), and the mixture was stirred overnight and filtered to remove an insoluble. Evaporation of the solvent from the filtrate gave a residue. Recrystallization of the resultant residue from acetonitrile gave 6-methyl-2-(3-nitrophenylamino)nicotinaldehyde (7.90 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642250B2
Source datasetuspto-grants-2003_11
ORD IDord-27e4b59d605b442da1fed7f5e375c992
Source noteuspto-grants-2003_11