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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254514Erstellt: 25. Oktober 2026

2-Bromobenzyl cyanide → 2-(2-Cyclopropylphenyl)acetonitrile

https://huagongshe.com/reaction/254514

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromobenzyl cyanideHCID 29625—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktTricyclohexylphosphineHCID 75806—
EduktCyclopropylboronic acidHCID 2760897—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt2-(2-Cyclopropylphenyl)acetonitrileHCID 5895177563,6%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 0.784 g (4 mmol) 2-bromophenyl-acetonitrile in 16 ml toluene were added 0.8 ml water, 0.412 g (4.8 mmol) cyclopropylboronic acid, 2.97 g (14 mmol) tribasic potassium phosphate, 0.1 12 g (0.4 mmol) tricyclohexylphosphine and 0.045 g (0.2 mmol) palladium(II) acetate. The reaction mixture was stirred at 100° C. for 2 days. The solvent was evaporated and the residue taken up in water and ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated. The residue was purified using column chromatography (SiO2, heptane/ethyl acetate 98:2) to yield 0.40 g of (2-cyclopropyl-phenyl)-acetonitrile as a light-yellow oil that was used directly for the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07875645B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-4d171b5178dd4365b39a40fdf193045c
Quellennotizuspto-grants-2011_01