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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063283Generated: October 31, 2026

Ethyl 3-methyl-4-(methylamino)-1-piperidinecarboxylate → N,3-Dimethylpiperidin-4-amine

https://huagongshe.com/reaction/1063283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-methyl-4-(methylamino)-1-piperidinecarboxylateHCID 15725099—
SolventSodium HydroxideHCID 14798—
ProductN,3-Dimethylpiperidin-4-amineHCID 22278841—

Reaction Conditions

Temperature110 °C

Reaction Steps

1-Carbethoxy-4-methylamino-3-methylpiperidine (4.0 g, 18.34 mmol) was suspended in 5 M NaOH solution (15 ml), stirred at 110° C. for 24 hr, cooled, extracted with ethyl acetate, dried (Na2SO4) and concentrated to dryness to afford 4-methylamino-3-methyl-piperidine. Yield 1.8 g (77%), C7H16N2, m/z 129 (M+1), PMR (CDCl3): 0.92 (dd, 3H), 1.54 (m, 1H), 2.12 (m, 2H), 2.38 (s, 3H), 2.6 (m, 1H), 2.8 (m, 1H), 3.02 (m, 1H), 3.42 (m, 1H), 3.68 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-34de939bd94e44aaa01c207d3be4b240
Source noteuspto-grants-2005_11