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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746896Generated: October 25, 2026

Ethylamine hydrochloride → 4-Ethylamino-1-carbethoxy-3,5-dimethylpiperidine

https://huagongshe.com/reaction/746896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamine hydrochlorideHCID 11198—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Carbethoxy-3,5-dimethyl-4-piperidinoneHCID 22278887—
SolventMethanolHCID 887—
Product4-Ethylamino-1-carbethoxy-3,5-dimethylpiperidineHCID 22278905—

Reaction Steps

Powdered KOH (2.8 g, 50 mmol) was added in portions to the stirred solution of ethylamine hydrochloride (4.0 g, 50 mmol) in methanol (50 ml) and 1-carbethoxy-3,5-dimethyl-4-piperidinone (5.0 g, 25.12 mmol) obtained by a procedure as described in Example 25 (Step-1), was added to it. The resulting reaction mixture was stirred for 6 hr. A solution of sodium cyanoborohydride (1.6 g, 25.12 mmol) in methanol (10 ml) was added dropwise to it and stirring was continued for 16 hr. The reaction mixture was concentrated to dryness. The obtained residue was dissolved in water and extracted with chloroform. Chloroform layer was extracted with 50% HCl and acid layer was basified with KOH (20%) solution. The oil thus separated was extracted with chloroform, dried (Na2SO4) and concentrated to give Mixtures A+B of 4-ethylamino-1-carbethoxy-3,5-dimethylpiperidine as an oil. Yield 5.6 g (97.7%), C12H24N2O2, m/z 229 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393957B2
Source datasetuspto-grants-2008_07
ORD IDord-b6c75eaef19b4011bfa22f2693602066
Source noteuspto-grants-2008_07