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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802748Generated: November 2, 2026

(2-Ethyl-pyrazolo[1,5-a]pyridin-3-yl)methanol → 2-Ethyl-pyrazolo[1,5-a]pyridine-3-carbaldehyde

https://huagongshe.com/reaction/1802748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Ethyl-pyrazolo[1,5-a]pyridin-3-yl)methanolHCID 57899265—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product2-Ethyl-pyrazolo[1,5-a]pyridine-3-carbaldehydeHCID 2346939598.3%

Reaction Steps

To a solution of (2-ethyl-pyrazolo[1,5-a]pyridin-3-yl)-methanol (9.67 g, 54.9 mmol) in tetrahydrofuran (500 mL) was added MnO2 (23.88 g, 274.5 mmol, 85%, dried in oven at 120° C. for 16 h) and stirred at the reflux temperature for 1.5 h. The reaction mixture was filtered through a Celite pad, and concentrated under reduced pressure to give 9.4 g (98%) of product, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349883B2
Source datasetuspto-grants-2013_01
ORD IDord-b70903b3d4be48d098045ba1c3c447e8
Source noteuspto-grants-2013_01