HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854130Generated: October 29, 2026
Hydrochloric Acid → HCID 178463142, compound
https://huagongshe.com/reaction/854130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylhydrazine | HCID 29062 | — |
| Reactant | Ethyl 2-methyl-4,4,4-trifluoroacetoacetate | HCID 2737204 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178463142 | HCID 178463142 | 72.1% |
Reaction Steps
To a solution of 1.2 g (20.0 mmol) of ethylhydrazine in 20 ml of ethanol was added dropwise under stirring 4.4 g (20.0 mmol) of ethyl 4,4,4-trifluoro-2-methyl-3-oxobutanoate under ice-cooling so that the temperature in the reaction system did not exceed 10° C. After the dropwise addition, the whole was stirred at room temperature for 30 minutes. Then, 1 ml of concentrated hydrochloric acid was added into the reaction solution, followed by 2 days of stirring under refluxing. After the completion of the reaction was confirmed, the solvent was removed by evaporation under reduced pressure. Water was added to the residue, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and saline, successively, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the residue was washed with n-hexane to obtain 2.8 g (yield: 71.8%) of 1-ethyl-5-hydroxy-4-methyl-3-trifluoromethyl-1H-pyrazole as white crystals (melting point: 150 to 152° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256298B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-66e9e2f25c484925a6feb167904cece1 |
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| Source note | uspto-grants-2007_08 |
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