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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1360432Erstellt: 24. Oktober 2026

Sodium Iodide → 4-(4-bromo-5-cyano-2-ethyl-2H-pyrazol-3-yl)butyl acetate

https://huagongshe.com/de/reaction/1360432

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktDimethylformamideHCID 6228—
EduktPotassium AcetateHCID 517044—
Edukt4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrileHCID 66958265—
LösungsmittelWaterHCID 962—
Produkt4-(4-bromo-5-cyano-2-ethyl-2H-pyrazol-3-yl)butyl acetateHCID 6695863680,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Potassium acetate (1.69 g, 17.2 mmol), sodium iodide (255 mg, 1.7 mmol), and DMF (17 mL) were added to 4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrile (1.0 g, 3.4 mmol, prepared as described in Parts A-E of Example 19), and the reaction was heated at 100° C. for two hours under a nitrogen atmosphere and allowed to cool to ambient temperature. Water was added, and the resulting mixture was extracted with diethyl ether. The combined extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by chromatography on a HORIZON HPFC system (40+M cartridge, eluting with hexanes/ethyl acetate in a gradient from 90:10 to 60:40) to provide 0.86 g of 4-(4-bromo-5-cyano-2-ethyl-2H-pyrazol-3-yl)butyl acetate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07879849B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-281e0706cfe1425eaca93023ce1cf1c4
Quellennotizuspto-grants-2011_02