Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419689Generated: November 2, 2026

Hydrazine, (4-chlorophenyl)-, hydrochloride (1:1) → Ethyl 1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/1419689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
ReactantEthyl 2-formyl-3-oxopropanoateHCID 11029955—
SolventEthanolHCID 702—
ProductEthyl 1-(4-chlorophenyl)-1H-pyrazole-4-carboxylateHCID 1380215749%

Reaction Steps

A solution of carbethoxymalonaldehyde (0.8 g, 5.55 mmol; obtained according to Panizzi, L. Gazz.Chim.Ital., 1946, 76, 56) in ethanol (25 mL) was treated with 4-chlorophenylhydrazine hydrochloride (1.0 g, 5.55 mmol) at reflux for 5 h. The resulting reddish mixture was concentrated to an oil that was purified by flash chromatography to give ethyl 1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate (0.68 g, 49%) as a white solid: mp 127°-128° C.; 1H NMR (80 MHz, CDCl3) δ (TMS) 8.37 (s, 1H, pyrazole), 8.09 (s, 1H, pyrazole), 7.67 (dt, Jt =2, Jd =9, 2H, arom), 7.44 (dt,Jt =2, Jd =9, 2H, arom), 4.35 (q, J=7, 2H, OCH2), 1.38 (t, J=7, 3H, OCH2CH3). Analysis calculated for C12H11ClN2O2 : C 57.50; H 4.42; N 11.17. Found: C 57.49; H 4.46; N 11.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05888941
Source datasetuspto-grants-1999_03
ORD IDord-7f00b2e71fd749db9f86450ca1320e4f
Source noteuspto-grants-1999_03