Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1487937Erstellt: 25. Oktober 2026

Pyrazole → 1-(4-bromophenyl)-1H-pyrazole

https://huagongshe.com/reaction/1487937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrazoleHCID 1048—
EduktN,N'-DimethylethylenediamineHCID 8070—
EduktCesium carbonateHCID 10796—
Edukt1-Bromo-4-iodobenzeneHCID 11522—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-(4-bromophenyl)-1H-pyrazoleHCID 1044356494,4%

Reaktionsbedingungen

Temperatur82 °C

Reaktionsschritte

Into a 100-mL round-bottom flask, which was purged and maintained with an inert atmosphere of nitrogen, was placed a mixture of 1-bromo-4-iodobenzene (2.82 g, 9.97 mmol), 1H-pyrazole (680 mg, 9.99 mmol), CuI (380 mg, 2.00 mmol), DMEDA (430 μL, 4.00 mmol, 0.40 equiv), Cs2CO3 (6.52 g, 20.00 mmol) an CH3CN (40 mL). The resulting mixture was stirred overnight at 82° C. After cooling to ambient temperature, the solids were removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:12) as the eluent to yield the title compound as a white solid (2.1 g, 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09428502B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-79947f4bba6a4c42af0fa5cabd864385
Quellennotizuspto-grants-2016_08