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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746852Erstellt: 25. Oktober 2026

Ethylamine hydrochloride → 1-Carbethoxy-4-ethylamino-3-methylpiperidine

https://huagongshe.com/reaction/746852

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylamine hydrochlorideHCID 11198—
EduktPotassium HydroxideHCID 14797—
EduktSodium cyanoborohydrideHCID 5003444—
EduktEthyl 3-methyl-4-oxopiperidine-1-carboxylateHCID 15075657—
LösungsmittelMethanolHCID 887—
Produkt1-Carbethoxy-4-ethylamino-3-methylpiperidineHCID 22278900—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ethylamine hydrochloride (5 g, 61.34 mmol) was added to the stirred solution of 1-carbethoxy-3-methyl-4-piperidone (3.5 g, 18.9 mmol) obtained as described in Preparation 1, in methanol (30 ml) followed by 3.43 g (61.34 mmol) KOH. Stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (1.4 g, 22.22 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 16 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH ˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and concentrated to dryness to give 1-carbethoxy-4-ethylamino-3-methylpiperidine. Yield 2.3 g (54%), C11H22N2O2, m/z 215 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07393957B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-4a81c61121f24ec5a460f8bc5630faca
Quellennotizuspto-grants-2008_07