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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2232395Erstellt: 27. Oktober 2026

Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)- → 1-(4-Aminophenyl)-4-(4-pyridyl)piperazine

https://huagongshe.com/reaction/2232395

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)-HCID 10924082—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt1-(4-Aminophenyl)-4-(4-pyridyl)piperazineHCID 1089046158,3%

Reaktionsschritte

A mixture of 1-(4-nitrophenyl)-4-(4-pyridyl)piperazine (2.07 g) in ethanol (100 ml) was hydrogenated at room temperature under a pressure of 2 bars in the presence of 10% palladium on charcoal (0.25 g). When reduction was complete, the catalyst was filtered off and the filtrate was evaporated. The residue was crystallised from methanol/ethyl acetate to give 1-(4-aminophenyl)-4-(4-pyridyl)piperazine (1.08 g), m.p. 210°-211° C. Found: C,70.47; H,7.07; N,21.56. C15H18N4 requires: C,70.83; H,7.13; N,22.03%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04788196
Quelldatensatzuspto-grants-1988_11
ORD IDord-724f0bbbf4eb4edaa1696d9bcefb874d
Quellennotizuspto-grants-1988_11