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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1387776Erstellt: 25. Oktober 2026

Water → 1-[2-(4-Nitrophenyl)ethyl]piperidine

https://huagongshe.com/reaction/1387776

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPiperidineHCID 8082—
EduktPotassium CarbonateHCID 11430—
Edukt4-Nitrophenethyl bromideHCID 79266—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[2-(4-Nitrophenyl)ethyl]piperidineHCID 220573—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

In DMF (100 ml) was dissolved 4-(2-bromoethyl)nitro-benzene (25.0 g), and to the solution were added piperidine (12.9 ml) and potassium carbonate (18.0 g). The mixture was stirred at 70° C. for 15 hours, and to the mixture was added water (900 ml), and then the mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate) to give 1-[2-(4-nitro-phenyl)ethyl]piperidine (24.8 g) as orange oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06268354B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-08fe3290b2de451e933668c7389e859d
Quellennotizuspto-grants-2001_07