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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1171633Erstellt: 26. Oktober 2026

Benzaldehyde → (E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-one

https://huagongshe.com/reaction/1171633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktPyrrolidineHCID 31268—
Edukt1-Tritylpiperidin-4-oneHCID 2748414—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(E)-3-Benzylidene-1-(triphenylmethyl)piperidin-4-oneHCID 6876571274%

Reaktionsschritte

To a solution of 1-(triphenylmethyl)piperidin-4-one (4.22 g) in benzene (50 ml) was added pyrrolidine (1.02 ml) at room temperature, and the resulting mixture was refluxed for 3 hours. After cooling to room temperature, benzaldehyde (1.26 ml) was added to the reaction mixture, and the resulting mixture was furthermore refluxed for 2 hours. After refluxing, the reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:3) as the eluent to afford the title compound (3.92 g, yield: 74%) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07829580B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-2834e8323229450fa7d7f6c49b06546f
Quellennotizuspto-grants-2010_11