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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615669Generated: November 1, 2026

Water → Imidazo(1,2-a)pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1615669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantImidazo[1,2-a]pyridin-2-ylmethanolHCID 2795540—
CatalystHCID 178418406HCID 178418406—
SolventEthanolHCID 702—
ProductImidazo(1,2-a)pyridine-2-carbaldehydeHCID 496125715.4%

Reaction Steps

To a solution of imidazo[1,2-a]pyridin-2-ylmethanol (3.0 g, 20 mmol) in EtOH (50 mL) was added manganese (IV) oxide (8.8 g, 100 mmol). The mixture was refluxed for 2 days. After cooling to room temperature, the mixture was filtered through Celite, and the filtrate was concentrated. The residue was purified by reverse phase column chromatography (eluting with acetonitrile in water 25% v/v, with 0.01% NH3. H2O) to afford the title compound (0.45 g, 15% yield) as a yellow solid. ESI MS: m/z 147 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-4a19075232f043c2b488e9527d3f5541
Source noteuspto-grants-2014_07