Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874595Generated: October 29, 2026

Methanol → (2-Trifluoromethylpyrazolo[1,5-a]pyridin-3-yl)methanol

https://huagongshe.com/reaction/874595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylateHCID 68088690—
SolventTetrahydrofuranHCID 8028—
Product(2-Trifluoromethylpyrazolo[1,5-a]pyridin-3-yl)methanolHCID 67056932100%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 2.8 g (11 mmol) of ethyl 2-trifluoromethylpyrazolo[1,5-α]pyridine-3-carboxylate in 50 ml of tetrahydrofuran is added dropwise to a suspension of 0.5 g (12 mmol) of lithium aluminum hydride in 45 ml of tetrahydrofuran. The reaction medium is then stirred at 70° C. for 3 h. After dropwise addition of 2.5 ml of methanol and then of 1.8 ml of an aqueous solution of sodium hydroxide having a concentration of 2N, the reaction medium is stirred for 20 min at ambient temperature and then filtered. The filtrate is dried over magnesium sulfate, filtered and concentrated under vacuum. 2.3 g (100%) of (2-trifluoromethylpyrazolo[1,5-α]pyridin-3-yl)methanol are obtained in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-2bf8ddeb56ce4ad7b04c197b1b62429e
Source noteuspto-grants-2015_03