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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1063284Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1063284

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
PatentnummerUS06964966B2
Quelldatensatzuspto-grants-2005_11
ORD IDord-862c9e1624514928a44601e76a9cda7d
Quellennotizuspto-grants-2005_11