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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178499156 | HCID 178499156 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Ethyl-3-(pentafluoroethyl)-4-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946234B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-9c85271981d1488c92b3975492eb27aa |
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| Source note | uspto-grants-2015_02 |
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