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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216508Generated: October 30, 2026

Cyclohexylhydrazine hydrochloride → Ethyl 1-cyclohexyl-5-(4-benzyloxyphenyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/2216508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylhydrazine hydrochlorideHCID 207836—
ReactantHCID 178473090HCID 178473090—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductEthyl 1-cyclohexyl-5-(4-benzyloxyphenyl)-1H-pyrazole-3-carboxylateHCID 1132717198.6%

Reaction Steps

The butenoate 1.2 (5.00 g, 15.3 mmol) and cyclohexylhydrazine hydrochloride (2.77 g, 18.4 mmol) were heated at refluxed in EtOH (60 ml) for 2 h. Concentration in vacuo resulted in formation of a solid which was suspended in EtOAc and filtered through a 1″ pad of SiO2, elution with ethyl acetate. The filtrate was concentrated to afford 6.10 g (98%) of the desired pyrazole ester 1.3. MS (ESI) 405.4 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112601B2
Source datasetuspto-grants-2006_09
ORD IDord-79572d6347054e7aa43d076ebd28c047
Source noteuspto-grants-2006_09