HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353568Generated: November 1, 2026
Lithium Hydroxide → 5-tert-Butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid
https://huagongshe.com/reaction/2353568
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 5-tert-Butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester | HCID 57418554 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-tert-Butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid | HCID 57418556 | 96% |
Reaction Steps
To 5-tert-butyl-2-p-tolyl-2H-pyrazole-3-carboxylic acid ethyl ester (0.5 g, 1.75 mmol) in a 40 mL scintillation vial was added 2 mL THF and 2 mL 1N LiOH. The reaction was heated at 50° C. for 1 hr after which the reaction mixture was concentrated under vacuum and the crude residue was diluted with 5 mL 1N HCl. The reaction slurry was then extracted with DCM (3×25 mL) and the combined organic layers were washed with brine (10 mL) and dried over MgSO4. The resulting solution was concentrated under vacuum to yield the desired product (0.432 g, 96%) in >95% purity. The isolated material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749999B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-646527e9e7fc4a6da00a7e2cdd4fef1c |
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| Source note | uspto-grants-2010_07 |
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