HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799437Generated: November 1, 2026
Potassium trimethylsilanolate → 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid
https://huagongshe.com/reaction/1799437
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium trimethylsilanolate | HCID 23668039 | — |
| Reactant | ethyl 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate | HCID 59516077 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | HCID 43259438 | 73.3% |
Reaction Steps
Potassium trimethylsilanolate (3.32 g, 23.28 mmol) was added in one portion to ethyl 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate (Intermediate #126) (2.4 g, 7.76 mmol), in THF (50 mL), under nitrogen. The resulting suspension was stirred at room temperature for 3 hours. The reaction mixture was evaporated to dryness and redissolved in EtOAc (100 mL), and washed sequentially with 0.1M HCl (50 mL), water (50 mL), and saturated brine (50 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude solid was triturated with isohexane to give a solid which was collected by filtration and dried under vacuum to give 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid (1.600 g, 73.3%) as a orange solid. Used directly in next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344016B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-84443da759354c7a92f3043ce7267fa7 |
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| Source note | uspto-grants-2013_01 |
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