HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12893Generated: October 25, 2026
Cyclohexylhydrazine hydrochloride → HCID 63235160, compound
https://huagongshe.com/reaction/12893
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylhydrazine hydrochloride | HCID 207836 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Butanoic acid, 2-[(dimethylamino)methylene]-4,4,4-trifluoro-3-oxo-, ethyl ester | HCID 53979199 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 63235160 | HCID 63235160 | 58.5% |
Reaction Steps
Cyclohexyl-hydrazine hydrochloride (0.276 g, 1.59 mmol, CAS #24214-73-1, purchased from Aldrich), 2-dimethylaminomethylene-4,4,4-trifluoro-3-oxo-butyric acid ethyl ester (0.459 g, 1.67 mmol) and anhydrous sodium acetate (0.188 g, 2.29 mmol) were combined in ethanol (2.9 mL) and heated at 70° C. for 15 hours. After cooling to room temperature, the reaction mixture was partitioned between methylene chloride and water. The organic phase was washed with water and brine. Each aqueous phase was back extracted with a second portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. Purification by flash chromatography, eluting with a 5-40% ethyl acetate-hexanes gradient, yielded 1-cyclohexyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (0.270 g, 55%). Mass spectrum: m/z: 291.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728029B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-ad7362163d764e3488d83dde6ee65506 |
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| Source note | uspto-grants-2010_06 |
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