HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49641Generated: October 25, 2026
Hydrochloric Acid → 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid
https://huagongshe.com/reaction/49641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Pyrazole-4-carboxylic acid, 1-methyl-3-(trifluoromethyl)-, ethyl ester | HCID 2782970 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid | HCID 2775665 | 98.4% |
Reaction Steps
50 g of ethyl 1-methyl-3-trifluoromethyl-4-pyrazolecarboxylate were initially charged with 177 g of toluene and 54 g of 25% sodium hydroxide solution and heated to reflux for 15 hours. The cloudy reaction mixture was cooled to 50° C. and admixed with 69 g of water. The aqueous phase was adjusted to pH 1-2 at 30° C. by adding 83 g of 15% hydrochloric acid, and the product precipitated out of solution. The suspension was stirred for a further 30 minutes at room temperature and for 30 minutes at 0° C., and the crude product was then isolated and washed 3 times with 60 g each time of cold (<10° C.) water. After drying at room temperature and under reduced pressure, 43 g of 1-methyl-3-trifluoromethyl-4-pyrazolecarboxylic acid were obtained. This corresponds to a yield of 98% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706911B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-768d08ef2f7f472a83947b43f7b993f8 |
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| Source note | uspto-grants-2004_03 |
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