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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 2-trifluoromethylpyrazolo[1,5-a]pyridine-3-carboxylate | HCID 68088690 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Trifluoromethylpyrazolo[1,5-a]pyridin-3-yl)methanol | HCID 67056932 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115102B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-f1477196bf194b5dba857494b31a2c8f |
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| Source note | uspto-grants-2015_08 |
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