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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814863Generated: November 4, 2026

Potassium Hydroxide → 1-Carbethoxy-4-methylamino-3-ethylpiperidine

https://huagongshe.com/reaction/1814863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant1-Carbethoxy-3-ethyl-4-piperidoneHCID 22278851—
SolventMethanolHCID 887—
Product1-Carbethoxy-4-methylamino-3-ethylpiperidineHCID 22278883—

Reaction Conditions

Temperature0 °C

Reaction Steps

Methylamine hydrochloride (17 g, 252 mmol) was added to the stirred solution of 1-carbethoxy-3-ethyl-4-piperidone (10 g, 50 mmol) in methanol (150 ml) followed by 14.1 g (252 mmol) KOH. Stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (4.72 g, 75 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 12 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 crude 1-carbethoxy-4-methylamino-3-ethylpiperidine. The obtained crude 1-carbethoxy-4-methylamino-3-ethylpiperidine was suspended in 7 M NaOH solution (50 ml), stirred at 110° C. for 230 hr, cooled, extracted with ethyl acetate, dried (Na2SO4) and concentrated to dryness to afford 4-methylamino-3-ethyl-piperidine. Yield 3.5 g (50%), C8H18N2, m/z 142 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878713B2
Source datasetuspto-grants-2005_04
ORD IDord-6b51a8b28b9142bba9a20cc5c50eb962
Source noteuspto-grants-2005_04