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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57091Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/57091

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt3-Chloro-1-(pyridine-3-yl)-1H-pyrazole-5-carboxylic acid hydrochlorideHCID 118021782—
KatalysatorCopper oxideHCID 14829—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAmmonium HydroxideHCID 14923—
Produkt3-(3-chloro-1H-pyrazol-1-yl)pyridineHCID 6749954073,4%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434712B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-e057a9d09fff4e41a0af34e569f9968e
Quellennotizuspto-grants-2016_09