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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24928Erstellt: 24. Oktober 2026

4-Nitrobenzaldehyde → 4-(Azetidin-1-yl-methyl)-nitrobenzene

https://huagongshe.com/de/reaction/24928

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzaldehydeHCID 541—
EduktSodium cyanoborohydrideHCID 5003444—
EduktAzetidine hydrochlorideHCID 12308726—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(Azetidin-1-yl-methyl)-nitrobenzeneHCID 22569653—

Reaktionsschritte

6.2 g (41 mmol) of 4-nitrobenzaldehyde and 3.8 g (40.6 mmol) of azetidine-hydrochloride are dissolved in 120 ml of ethanol. 2.6 g (41 mmol) of sodium cyanoborohydride are added at 0° C. The mixture is slowly heated to ambient temperature and then stirred for 18 hours. Then the solvent is eliminated in vacuo, the residue is taken up in ethyl acetate and washed with water. The solvent is eliminated in vacuo and after chromatography of the residue on silica gel (ethyl acetate/methanol/NH4OH=95:5:0.5) a light brown oil is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855710B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-ebebe92616344816b517ea4dc75ba6dd
Quellennotizuspto-grants-2005_02