HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 270621Erstellt: 25. Oktober 2026
Triphenylphosphine → 2'-Acetyl[1,1'-biphenyl]-4-carbonitrile
https://huagongshe.com/reaction/270621
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 4-Chlorobenzonitrile | HCID 12163 | — |
| Edukt | 2-Acetylphenylboronic acid | HCID 2734309 | — |
| Edukt | Potassium phosphate, tribasic, monohydrate | HCID 22031701 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2'-Acetyl[1,1'-biphenyl]-4-carbonitrile | HCID 12188425 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07449574B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-6a8ed67d0e5942ddaf4af41eeb0a8c3e |
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| Quellennotiz | uspto-grants-2008_11 |
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