HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711672Generated: October 27, 2026
Lithium Hydroxide → 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acid
https://huagongshe.com/reaction/1711672
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | ethyl 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylate | HCID 67251871 | — |
| Solvent | Dioxane ethanol water | HCID 69104347 | — |
| Product | 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acid | HCID 67253105 | 94% |
Reaction Steps
Lithium hydroxide (62 mg, 2.6 mmol) was added to a solution of ethyl 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylate (0.21 g, 0.65 mmol) in dioxane-H2O-EtOH (1:1:1, 6 mL). The reaction mixture was stirred overnight at RT. The solution was concentrated and the residue was dissolved in H2O (2 mL). 3M HCl was added and the precipitate was collected by filtration and washed with water. The solid was dried under vacuum to obtain 3-tert-butyl-1-(quinolin-6-yl)-1H-pyrazole-5-carboxylic acid (0.18 g, 94% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.96 (dd, J=2.0, 4.0 Hz, 1H), 8.47 (dd, J=1.2, 8.4 Hz, 1H), 8.09 (m, 1H), 8.06 (s, 1H), 7.82 (dd, J=2.8, 9.2 Hz, 1H), 7.61 (dd, J=4.8, 8.8 Hz, 1H), 7.01 (s, 1H), 1.33 (s, 9H); MS (ESI) m/z: 296.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790756B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-0d8bbf5656364a99addf5d7d201e4ad1 |
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| Source note | uspto-grants-2010_09 |
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