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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1079392Erstellt: 26. Oktober 2026

Piperidine → Piperidine, 1-(4-nitrophenyl)-

https://huagongshe.com/reaction/1079392

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Eduktp-FluoronitrobenzeneHCID 9590—
LösungsmittelDimethylformamideHCID 6228—
ProduktPiperidine, 1-(4-nitrophenyl)-HCID 81049—

Reaktionsschritte

A solution of p-fluoronitrobenzene (31.8 ml) in dimethylformamide (200 ml) was ice-cooled and to this was added piperidine (60 ml) dropwise, followed by stirring with ice cooling for 2 hours. After the solvent was distilled off, the residual oily product was dissolved in ethyl acetate ester (200 ml), followed by washing in turn with aqueous saturated solution of sodium bicarbonate and water. Then, the solution was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was recrystallized from n-hexane to obtain N-(4-nitrophenyl)piperidine as yellow crystals (52.8 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05580883
Quelldatensatzuspto-grants-1996_12
ORD IDord-2cf7a327371f4730a5c5bfa29490dc36
Quellennotizuspto-grants-1996_12