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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773179Generated: November 2, 2026

Ethyl Acetate → 3-(3-chloro-1H-pyrazol-1-yl)pyridine

https://huagongshe.com/reaction/1773179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Chloro-1-(pyridine-3-yl)-1H-pyrazole-5-carboxylic acid hydrochlorideHCID 118021782—
CatalystCopper oxideHCID 14829—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAmmonium HydroxideHCID 14923—
Product3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 6749954073.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-Chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylic acid hydrochloride (1.00 g, 3.65 mmol) was stirred in N,N-dimethylformamide (10 mL). Copper(II) oxide (58.0 mg, 0.730 mmol) was added and the reaction was heated at 120° C. for 16 hours, at which point the reaction was ˜20% complete. Additional copper(II) oxide (112 mg, 1.46 mmol) was added and the reaction was stirred for 5 hours, at which point the reaction was complete by thin layer chromatography (TLC) [Eluent: ethyl acetate]. The mixture was diluted with ammonium hydroxide (NH4OH) and water and extracted with ethyl acetate. The organic layer was washed with 15% lithium chloride and concentrated to provide an orange solid. The residue was purified by flash column chromatography using ethyl acetate as eluent and the pure fractions were concentrated to afford the desired product as a white solid (481 mg, 69.7%). The spectral characterization was in agreement with the product prepared previously.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255083B2
Source datasetuspto-grants-2016_02
ORD IDord-6d41e1ce0aef4c41949cfa394bf01b5b
Source noteuspto-grants-2016_02