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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238372Erstellt: 25. Oktober 2026

Ethanol → 1'-(4-Fluorophenyl)-2-methyl-1'H,2H-3,4'-bipyrazole

https://huagongshe.com/reaction/238372

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt5-Iodo-1-methyl-1H-pyrazoleHCID 13334065—
Edukt1-(4-Fluorophenyl)pyrazole-4-boronic acidHCID 46738684—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt1'-(4-Fluorophenyl)-2-methyl-1'H,2H-3,4'-bipyrazoleHCID 8668487164,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Under a nitrogen atmosphere, a mixture of 5-iodo-1-methyl-1H-pyrazole (600 mg), [1-(4-fluorophenyl)-1H-pyrazol-4-yl]boronic acid (650 mg), tetrakistriphenylphosphine palladium (166 mg), 2 M sodium carbonate aqueous solution (2.9 mL), ethanol (3.0 mL) and toluene (6.0 mL) was stirred at 100° C. for 4 hours. Thereafter, water was added to the reaction solution, and the obtained mixture was then extracted with ethyl acetate. The organic layer was concentrated under a reduced pressure, and the residue was then purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=9:1 to ethyl acetate), so as to obtain the title compound (450 mg) in the form of a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642626B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-ffefd9914333427893e53e9a6ac5a748
Quellennotizuspto-grants-2014_02