Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2218856Erstellt: 26. Oktober 2026

Tetrahydrofuran → 1-[4-[2-(4,4-Diethylcyclohexyl)phenyl]piperazin-1-yl]butan-1-one

https://huagongshe.com/reaction/2218856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktTriethylamineHCID 8471—
EduktButyryl chlorideHCID 8855—
EduktSodium BicarbonateHCID 516892—
Edukt1-[2-(4,4-Dimethylcyclohexyl)phenyl]piperazineHCID 23142224—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-[4-[2-(4,4-Diethylcyclohexyl)phenyl]piperazin-1-yl]butan-1-oneHCID 23142306—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1-[2-(4,4-dimethylcyclohexyl)phenyl]piperazine (30 mg, 0.10 mmol) produced in Example (83a) in tetrahydrofuran (1 mL) was added triethylamine (15 mg, 0.15 mmol), followed by stirring at an external temperature of 0° C. Butyryl chloride (0.015 mL, 0.14 mmol) was added to the reaction mixture while stirring, and the stirring was continued for 9 hours and 30 minutes at an external temperature of 0° C. Saturated aqueous solution of sodium hydrogencarbonate was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with water and filtered through Celite, and the filtrate was concentrated. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 27 mg of the title compound as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07410971B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-5fb9d8f480d444178b075c450a11506a
Quellennotizuspto-grants-2008_08