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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1859629Erstellt: 24. Oktober 2026

Ethyl Acetate → 4-n-Butyl-1-[4-(2ethoxyphenyl)-4-oxo-1-butyl]piperidine

https://huagongshe.com/de/reaction/1859629

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktBenzene, 1-ethoxy-2-iodo-HCID 136415—
Edukt4-(4-Butylpiperidin-1-YL)butanenitrileHCID 18626385—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-n-Butyl-1-[4-(2ethoxyphenyl)-4-oxo-1-butyl]piperidineHCID 994944434%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

In a 10 mL oven-dried flask was added Mg turnings (94 mg, 3.8 mmol) which was activated by the use of a heat-gun under vacuum. Under inert atmosphere was added a suspension of 1-ethoxy-2-iodobenzene (0.71 g, 2.9 mmol) in Et2O (3 mL) and the reaction mixture was allowed to reflux for 3 hours. Compound 4 (0.40 g, 1.9 mmol) dissolved in CH2Cl2 (3 mL) was added and the mixture was stirred at 40° C. for additional 3 hours. The reaction mixture was quenched by addition of H2SO4 (10 mL, 2 M) and left stirring overnight at room temperature, followed by addition of NaOH (20 mL, 2 M) until basic conditions. The reaction mixture was extrated with ethyl acetate (3×50 mL) ) and the combined organic phases are washed with brine (10 mL) and NaOH (10 mL, 2 M), and the combined organic phases were dried (MgSO4) and evaporated to dryness to produce 0.60 g of crude 18. The crude product was subjected to CC [eluent:Tol:EtOAc (1:1)] to give pure 18 (0.32 g, 34%); LC-MS [M+H]+ 331 (cald. 331.5).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06528529B1
Quelldatensatzuspto-grants-2003_03
ORD IDord-b685cb8ea2eb4b07b9d171232fefc84c
Quellennotizuspto-grants-2003_03