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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509939Generated: October 30, 2026

(5-Fluoro-2-methoxypyridin-3-yl)methanol → 5-Fluoro-2-methoxynicotinaldehyde

https://huagongshe.com/reaction/509939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Fluoro-2-methoxypyridin-3-yl)methanolHCID 44754796—
CatalystHCID 178418406HCID 178418406—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-2-methoxynicotinaldehydeHCID 2267832357%

Reaction Steps

To (5-fluoro-2-methoxy-pyridin-3-yl)-methanol (36, 8 g, 50.9 mmol) in 300 mL of ethyl acetate, manganese(IV) oxide (39.8 g, 458 mmol) was added and the mixture stirred at room temperature overnight. The reaction mixture was filtered through celite, and the celite bed rinsed with ethyl acetate. The filtrate was concentrated under vacuum, then passed through a plug of silica, eluting with 50% ethyl acetate in heptane to provide the desired compound as a light yellow solid (37, 4.5 g, 29.0 mmol, 57.0% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096593B2
Source datasetuspto-grants-2015_08
ORD IDord-973f28eabc2548f0814f563d2ede27d0
Source noteuspto-grants-2015_08