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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12893Generated: October 25, 2026

Cyclohexylhydrazine hydrochloride → HCID 63235160, compound

https://huagongshe.com/reaction/12893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylhydrazine hydrochlorideHCID 207836—
ReactantSodium AcetateHCID 517045—
ReactantButanoic acid, 2-[(dimethylamino)methylene]-4,4,4-trifluoro-3-oxo-, ethyl esterHCID 53979199—
SolventEthanolHCID 702—
ProductHCID 63235160HCID 6323516058.5%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-ad7362163d764e3488d83dde6ee65506
Source noteuspto-grants-2010_06