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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1847171Erstellt: 27. Oktober 2026

Aniline → 2-(Phenylamino)benzonitrile

https://huagongshe.com/reaction/1847171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktCesium carbonateHCID 10796—
Edukt2-BromobenzonitrileHCID 16272—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-(Phenylamino)benzonitrileHCID 25288081,6%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a suspension of 2-bromobenzonitrile (1.5 g, 8.2 mmol), aniline (1.1 g, 12.4 mmol), Xantphos (0.7 g, 1.2 mmol) and cesium carbonate (5.4 g, 16.5 mmol) in dioxane (50 mL) was added Pd2dba3 (375 mg, 0.4 mmol) at rt under N2. The reaction was stirred at 90° C. for 8 h. The reaction mixture was filtered and concentrated. Purification by silica gel chromatography (PE:EtOAc=200:1) gave 1.3 g (81%) of the title compound as a yellow oil. 1H NMR (300 MHz, CDCl3): δ 6.36 (1H, br s), 6.86 (1H, td, J=0.9, 7.8 Hz), 7.13-7.18 (4H, m), 7.36-7.41 (3H, m), 7.51 (1H, dd, J=1.8, 7.8 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08952151B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-0521e3ac04eb4b8ba8d898a727f5f14a
Quellennotizuspto-grants-2015_02