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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510684Generated: November 4, 2026

(5-Fluoro-6-methoxypyridin-3-yl)methanol → 5-Fluoro-6-methoxypyridine-3-carbaldehyde

https://huagongshe.com/reaction/1510684

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Fluoro-6-methoxypyridin-3-yl)methanolHCID 57815441—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product5-Fluoro-6-methoxypyridine-3-carbaldehydeHCID 4475478490%

Reaction Steps

To a solution of 0.54 g of (5-fluoro-6-methoxypyridin-3-yl)methanol in 5 mL of dichloromethane, 1.5 g of manganese dioxide was added. The mixture was stirred at room temperature for 3 hours, thereto were then added 0.89 g of manganese dioxide and 4 mL of dichloromethane, and the mixture was stirred for 1 hour. Thereto were further added 1.5 g of manganese dioxide and 2 mL of dichloromethane, and the mixture was stirred at room temperature for 2 hours 30 minutes. After leaving overnight, the insoluble substance was filtered off, and the filtration residue was washed with chloroform. The solvent was distilled off under reduced pressure to obtain 0.48 g of 5-fluoro-6-methoxynicotinaldehyde as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211908B2
Source datasetuspto-grants-2012_07
ORD IDord-25887b04068c42b1beab8741d99a6679
Source noteuspto-grants-2012_07