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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160564Generated: November 1, 2026

Potassium trimethylsilanolate → 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1160564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium trimethylsilanolateHCID 23668039—
Reactantethyl 1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 59516077—
SolventTetrahydrofuranHCID 8028—
Product1-(4-cyanophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 4325943873.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816391B2
Source datasetuspto-grants-2010_10
ORD IDord-c98e08c8ddbb4ce98287cb8befa3aa29
Source noteuspto-grants-2010_10