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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270621Erstellt: 25. Oktober 2026

Triphenylphosphine → 2'-Acetyl[1,1'-biphenyl]-4-carbonitrile

https://huagongshe.com/reaction/270621

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt4-ChlorobenzonitrileHCID 12163—
Edukt2-Acetylphenylboronic acidHCID 2734309—
EduktPotassium phosphate, tribasic, monohydrateHCID 22031701—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTolueneHCID 1140—
Produkt2'-Acetyl[1,1'-biphenyl]-4-carbonitrileHCID 12188425—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Bis(triphenylphosphine)palladium dichloride (PdCl2(PPh3)2) (0.6 g, 0.86 mmol), triphenylphosphine (0.44 g, 1.74 mmol), (2-acetylphenyl)boronic acid (6 g, 3.76 mmol) and tripotassium phosphate hydrate (16 g, 7.54 mmol) were placed in a flask. Nitrogen was blown into the flask and then the flask was filled with toluene (40 ml) and 4-chlorbenzonitrile (4 g, 2.90 mmol). The reaction mixture was stirred at 80° C. for 4 hours. The reaction mixture was cooled and washed with water. The organic layer was dried over sodium sulfate and then the solvent was evaporated. The product, 2′-acetyl-4-biphenylcarbonitrile (5a) was purified by a column (hexane/ethyl acetate=8/1). Yield: 3.3 g (51%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449574B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-6a8ed67d0e5942ddaf4af41eeb0a8c3e
Quellennotizuspto-grants-2008_11