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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 887343Erstellt: 25. Oktober 2026

Ammonium Acetate → tert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/887343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium AcetateHCID 517165—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—
LösungsmittelMethanolHCID 887—
LösungsmittelSodium HydroxideHCID 14798—
Produkttert-Butyl 4-(1-aminoethyl)piperidine-1-carboxylateHCID 2264729590%

Reaktionsschritte

A mixture of tert-butyl 4-acetylpiperidine-1-carboxylate (145 g, 0.64 mol) and ammonium acetate (225 g, 2.9 mol) in methanol (2 L) was stirred at room temperature for 1.5 hours. Sodium cyanoborohydride (30 g, 0.48 mol) was added in one portion and the stirring was continued overnight at room temperature. The reaction mixture was poured in 2N aq. NaOH (2 L) and extracted with dichloromethane (2×1 L). The combined extracts were washed with water (1 L), brine (0.3 L), and evaporated to dryness. The residue was dissolved in TBME (1.5 L), dried over sodium sulfate, filtered, and evaporated to dryness under reduced pressure. The residue was purified by bulb to bulb distillation at 180° C. and 0.1 mbar to afford the title compound as a colorless oil that partly solidified upon standing (131 g, 90% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247421B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-1892656c66ba4a8e84e873ddd015b516
Quellennotizuspto-grants-2012_08