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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540746Generated: October 25, 2026

Triethylamine → 3-(1-ethyl-5-oxo-2,5-dihydro-1H-pyrazol-3-yl)benzonitrile

https://huagongshe.com/reaction/540746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydrazine, ethyl-, ethanedioate (1:1)HCID 96181—
ReactantEthyl 3-(3-cyanophenyl)-3-oxopropanoateHCID 11622629—
SolventEthanolHCID 702—
Product3-(1-ethyl-5-oxo-2,5-dihydro-1H-pyrazol-3-yl)benzonitrileHCID 67111059122.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

Ethyl hydrazine oxalate (15.6 g, 104 mmol, 1.50 equiv) was added to a solution of ethyl 3-(3-cyanophenyl)-3-oxopropanoate (15.0 g, 69.1 mmol, 1 equiv) and triethylamine (14.4 mL, 104 mmol, 1.50 equiv) in ethanol (345 mL). The reaction mixture was heated to 80° C. for 70 min, then was removed from heat an concentrated to ˜¼ volume by rotary evaporation. The residue was partitioned between ethyl acetate and water. The organic layer was washed with saturated aqueous sodium chloride solution, and the washed solution was dried over sodium sulfate. The dried solution was filtered, and the filtrate was concentrated to afford 3-(1-ethyl-5-oxo-2,5-dihydro-1H-pyrazol-3-yl)benzonitrile as a light-yellow solid (18.1 g) of sufficient purity to use in the next step without further purification. Calcd (M+1)+: 214.1. Found: 214.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871796B2
Source datasetuspto-grants-2014_10
ORD IDord-28619cae3ae042aa8bae253f32b8497b
Source noteuspto-grants-2014_10