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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 630Erstellt: 24. Oktober 2026

Benzonitrile, 4-bromo- → Tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/630

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzonitrile, 4-bromo-HCID 12162—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylateHCID 279551282,34%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To 4-bromobenzonitrile (.5 g, 2.75 mmol) dissolved in dry THF (10 mL) was added tert-butyl piperazine-1-carboxylate (0.512 g, 2.75 mmol), Sodium-t- butoxide (0.792 g, 8.24 mmol) and purged with N2 gas for 10 min followed by the addition of 2-(Dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl (0.131 g, 0.27 mmol)and Palladium II acetate (0.062 g, 0.27 mmol). The contents were further purged with N2 gas for further 10 min and heated at 85 °C for 2 h. The reaction mass was concentrated and the reside diluted with water and extracted with ethyl acetate . The combined organic extracts were washed with brine solution and dried over anhydrous sodium sulphate. The organic layer was evaporated under reduced pressure to obtain the crude product which was purified by 60-120 mesh silica gel column chromatography using 25% Ethyl acetate : Hexanes mixture to obtain tert-butyl 4-(4-cyanophenyl)piperazine-1-carboxylate (0.650 g, 82 %) as a white solid. m/z (ES+), M+ = 288.4

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-587e8b015ef542aa9ba95a064a0d6902
Quellennotiz750 AstraZeneca ELN dataset