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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 409672Erstellt: 24. Oktober 2026

1-Bromo-4-nitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/de/reaction/409672

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-nitrobenzeneHCID 11466—
Edukt1-BenzylpiperazineHCID 75994—
LösungsmittelWater methylene chlorideHCID 21908982—
Produkt1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-bromo-4-nitrobenzene (5 g, 24.8 mmol) and 1-benzylpiperazine (8.6 ml, 49.5 mmol, 2 equiv) is heated to 80° C. for 17 h. The reaction mixture is allowed to cool to RT, and is diluted with DCM/H2O. The layers are separated and the aqueous phase is extracted with DCM. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the residue by silica gel column chromatography (Hex/EtOAc, 1:1) affords the title compound as a yellow solid: ESI-MS: 298.3 [MH]+; tR=3.25 min (purity: 100%, system 1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08759517B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-58bd338a40824640897be00271babb1d
Quellennotizuspto-grants-2014_06