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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510702Generated: November 3, 2026

(4-Methoxy-5-methylpyridin-2-yl)methanol → 4-Methoxy-5-methylpyridine-2-carbaldehyde

https://huagongshe.com/reaction/1510702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxy-5-methylpyridin-2-yl)methanolHCID 15163463—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-Methoxy-5-methylpyridine-2-carbaldehydeHCID 5781540060%

Reaction Steps

To a solution of 0.13 g of (4-methoxy-5-methylpyridin-2-yl)methanol in 2 mL of dichloromethane, 0.14 g of manganese dioxide was added. The mixture was stirred for 6 hours while dividedly further adding 0.36 g of manganese dioxide at room temperature. The insoluble substance was filtered off, the solvent was distilled off under reduced pressure, and the resultant residue was purified by flash column chromatography using gradient elution of hexane:ethyl acetate=9:1 to 4:1 to obtain 77 mg of 4-methoxy-5-methylpyridine-2-carbaldehyde as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211908B2
Source datasetuspto-grants-2012_07
ORD IDord-2faaf52d03244563851aad2612426346
Source noteuspto-grants-2012_07