Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843071Generated: October 31, 2026

Hydrochloric Acid → 1-Ethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid

https://huagongshe.com/reaction/1843071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178499156HCID 178499156—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-Ethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidHCID 58542539—

Reaction Steps

0.23 g (0.72 mmol) of methyl 3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxylate and 0.3 g (2.2 mmol) of potassium carbonate are suspended in 7.0 ml of acetone and admixed with 0.12 ml of iodoethane (1.4 mmol). The reaction mixture is stirred overnight at room temperature. 1.1 ml (2.2 mmol) of 2N sodium hydroxide solution are added to the suspension. The solution is then stirred overnight at room temperature. The reaction mixture is diluted with water and adjusted to pH 2-3 with 1M hydrochloric acid. The aqueous reaction solution is extracted three times with ethyl acetate. The combined organic phases are dried over magnesium sulphate, filtered and concentrated by evaporation under reduced pressure on a rotary evaporator. This gives 0.22 g of 1-ethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid (91%) as a colourless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946234B2
Source datasetuspto-grants-2015_02
ORD IDord-9c85271981d1488c92b3975492eb27aa
Source noteuspto-grants-2015_02