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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517525Generated: October 30, 2026

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

https://huagongshe.com/reaction/517525

Reaction equation

Participants

RoleNameHCIDCharge
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

Temperature-70 °C

Reaction Steps

A solution of 2.8 g (10.8 mmol) of ethyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylate in 50 ml of tetrahydrofuran is added dropwise to a mixture of 0.5 g (11.9 mmol) of lithium aluminium hydride in suspension in 45 ml of tetrahydrofuran at −70° C. After stirring for 3 h at −70° C., the mixture is brought to ambient temperature, then 1.8 ml of a 2N aqueous sodium hydroxide solution is added. The mixture is filtered, dried over magnesium sulphate, filtered and concentrated. 2.3 g (100%) of (2-trifluoromethylpyrazolo[1,5-a]pyridin-3-yl)methanol are obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115102B2
Source datasetuspto-grants-2015_08
ORD IDord-f1477196bf194b5dba857494b31a2c8f
Source noteuspto-grants-2015_08