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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 576533Erstellt: 24. Oktober 2026

1-Phenyl-2-propen-1-one → 1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one

https://huagongshe.com/de/reaction/576533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Phenyl-2-propen-1-oneHCID 13028—
EduktPotassium HydroxideHCID 14797—
Edukt1,4-DioxaneHCID 31275—
Edukt1,3-Dimethyl-4-piperidoneHCID 107311—
LösungsmittelWaterHCID 962—
Produkt1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-oneHCID 6735711010,8%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

To a stirred solution of 1,3-dimethyl-piperidin-4-one (0.1 g, 0.787 mmol) in mixture of 1,4 dioxane (2 mL) and water (0.1 mL) was added crushed KOH (44 mg, 0.787 mmol). The reaction mixture was stirred at 25° C. for 10 min. To this was added 1-phenylprop-2-en-1-one (103 mg, 0.787 mmol) dropwise. The reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water (10 mL) and EtOAc (20 mL), the organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting crude product was purified by column chromatography on neutral alumina (eluted with EtOAc:Hexanes, 1:99) to afford 1,3-dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one as an oil (22 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040519B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-0c551d20fef6440ca1f200327530665c
Quellennotizuspto-grants-2015_05