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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063287Generated: October 26, 2026

Acetic Acid → 1-Carbethoxy-4-dimethylamino-3-methylpiperidine

https://huagongshe.com/reaction/1063287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 4-amino-3-methylpiperidine-1-carboxylateHCID 22278886—
SolventMethanolHCID 887—
Product1-Carbethoxy-4-dimethylamino-3-methylpiperidineHCID 22278865—

Reaction Steps

Paraformaldehyde (5.1 g) was added to the stirred solution of 4-amino-1-carbethoxy-3-methylpiperidine (3.5 g, 18.8 mmol) in methanol (100 ml) at 0° C. and sodium cyanoborohydride (1.7 g, 27.0 mmol) was added to it. Then, acetic acid (1 ml) was added to the resulting mixture and stirring was continued for 96 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-dimethylamino-3-methylpiperidine. Yield 3.5 g (88%), C11H22N2O2, m/z 215 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-29a5f829c0f641f5a621952cc3647b16
Source noteuspto-grants-2005_11