HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472148Generated: October 30, 2026
Methanol → (2-Trifluoromethylpyrazolo[1,5-a]pyridin-3-yl)methanol
https://huagongshe.com/reaction/472148
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| 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 (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633196B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-16c170a19a294032aaa88775dcaf38c5 |
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| Source note | uspto-grants-2014_01 |
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