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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250956Generated: October 26, 2026

(3,5-Dimethylpyridin-2-yl)methanol → 3,5-Dimethylpyridine-2-carbaldehyde

https://huagongshe.com/reaction/250956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3,5-Dimethylpyridin-2-yl)methanolHCID 10630548—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3,5-Dimethylpyridine-2-carbaldehydeHCID 18731683—

Reaction Steps

To a solution of (3,5-dimethyl-pyridin-2-yl)-methanol (2.12 g, 15.45 mmol) (Weidmann, K. et al. J. Med. Chem. 1992, 35, 438-450) in CH2Cl2 (50 mL) was added MnO2 (9.41 g, 108.18 mmol) and the reaction mixture was refluxed overnight. Then it was cooled and the mixture was filtered through a layer of celite. The filtrate was concentrated to afford a brown/yellow oil. Purification by flash column chromatography on silica gel using 30% EtOAc/hexane afforded 3,5-dimethyl-pyridine-2-carbaldehyde as a yellow oil (960 mg, 31% over 3 steps). 1H NMR (CDCl3) δ 2.39 (s, 3H), 2.62 (s, 3H), 7.41 (s, 1H), 8.47 (s, 1H), 10.15 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863293B2
Source datasetuspto-grants-2011_01
ORD IDord-727f3f24a0a64931b81c617c484e059c
Source noteuspto-grants-2011_01