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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2242948Erstellt: 25. Oktober 2026

Acetic Acid → [1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2242948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
Edukt4-(N-Boc-amino)piperidineHCID 723833—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelEthanolHCID 702—
Produkt[1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl esterHCID 6714736153%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of piperidin-4-yl-carbamic acid tert-butyl ester (10.0 g, 50.0 mmol, 1.0 equiv), 3-ethoxy-4-methoxy-benzaldehyde (10.8 g, 60.0 mmol, 1.2 equiv; commercially available) and acetic acid (11.4 mL, 12.01 g, 200.0 mmol, 4.0 equiv) in ethanol (40 mL) was heated by microwave irradiation to 100° C. for 5 min. Sodium cyanoborohydride (6.27 g, 100.0 mmol, 2.0 equiv), dissolved in ethanol (20 mL), was added and the reaction mixture heated by microwave irradiation to 100° C. for an additional time period of 5 min. The solvent was removed under reduced pressure and the crude reaction product extracted from a solution of 1 M NaOH (200 mL) with ethyl acetate (3×100 mL). The combined organic phases were dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with ethyl acetate to yield 9.71 g (53%) of the title compound as a white solid. MS (ISP): 365.3 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07674804B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-89c5b060abfb4b89a658be4d2b1d78f9
Quellennotizuspto-grants-2010_03