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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385564Generated: October 30, 2026

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

https://huagongshe.com/reaction/385564

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 numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-56330486ba3a4994a1b974a44941248d
Source noteuspto-grants-2013_02