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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 888561Erstellt: 24. Oktober 2026

Benzaldehyde → 2-(3-Bromo-phenyl)-3-phenyl-propionitrile

https://huagongshe.com/de/reaction/888561

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPotassium HydroxideHCID 14797—
Edukt(3-Bromophenyl)acetonitrileHCID 36023—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt2-(3-Bromo-phenyl)-3-phenyl-propionitrileHCID 5933198152%

Reaktionsschritte

A solution of 40% KOH (2.83 g in 5.0 ml of H2O) in ethanol (13 ml) was added to a solution of benzaldehyde (2.85 ml, 28.05 mmol) and 3-bromophenylacetonitrile (5 g, 25.50 mmol) in ethanol (9 ml). The reaction mixture was then stirred at room temperature for 2 hours and the precipitate was collected by suction filtration and washed with cold ethanol (6.68 g, 92%). The crude product (3.45 g, 12.14 mmol) was then dissolved in ethanol (35 ml) and heated to 65° C. Sodium borohydride (459 mg, 12.14 mmol) was added in portions and the reaction mixture was maintained at this temperature for a further 2 hours. Upon cooling, water (10 ml) was added and the solvent was removed under reduced pressure. The residue was partitioned between water (100 ml) and ethyl acetate (100 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated to afford the desired product (1.80 g, 52%), which was used without purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247576B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-b8d973987e364674877ad088b10f09a1
Quellennotizuspto-grants-2012_08