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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594258Generated: November 2, 2026

[6-(1H-pyrazol-1-yl)pyridin-2-yl]methanol → 6-(1H-Pyrazol-1-yl)-2-pyridinecarboxaldehyde

https://huagongshe.com/reaction/594258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[6-(1H-pyrazol-1-yl)pyridin-2-yl]methanolHCID 62255710—
CatalystManganese dioxideHCID 14801—
Solvent1,2-DichloroethaneHCID 11—
Product6-(1H-Pyrazol-1-yl)-2-pyridinecarboxaldehydeHCID 10511407—

Reaction Steps

A solution of (6-(1H-pyrazol-1-yl)pyridin-2-yl)methanol (295 mg; 1.68 mmol) in anh. DCE (6 ml) was treated with MnO2 (1.174 g; 13.51 mmol), and the resulting mixture was stirred at reflux, under nitrogen, for 2 h. After cooling to rt, the resulting reaction mixture was filtered over celite, and the separated solids were washed with DCM. The filtrate was concentrated to dryness under reduced pressure giving 6-(1H-pyrazol-1-yl)picolinaldehyde as an off-white solid. LC-MS (conditions C): tR=0.74 min.; [M+H]+: 173.88 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-bb17d829b40c4c1aad155d4dff028fb0
Source noteuspto-grants-2016_01