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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454001Generated: October 25, 2026

Formic Acid → ethyl (3R)-1-methylpiperidine-3-carboxylate

https://huagongshe.com/reaction/454001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantSodium HydroxideHCID 14798—
Reactantethyl (3R)-piperidine-3-carboxylateHCID 185582—
ReactantSodium BicarbonateHCID 516892—
SolventFormaldehydeHCID 712—
Productethyl (3R)-1-methylpiperidine-3-carboxylateHCID 73603673%

Reaction Steps

(R)-Ethyl nipecotate (5.7 g 365 mmol), (prepared by resolution of ethyl nipecotate by treatment with L(+)-tartaric acid as described in J. Org. Chem. 1991, (56), 1168), was dissolved in 38.5% aqueous formaldehyde solution (45 ml) and formic acid (90 ml) and the mixture heated at reflux for 18 hours. The mixture was allowed to cool and added dropwise to cooled saturated aqueous sodium hydrogen carbonate solution. The mixture was adjusted to pH12 by addition of sodium hydroxide and the mixture was extracted with methylene chloride. The organic extract was washed with brine, dried (MgSO4) and the solvent removed by evaporation to give (R)-ethyl 1-methylpiperidine-3-carboxylate (4.51 g, 73%) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-9aadfca64f224018952b4241356f9dbd
Source noteuspto-grants-2013_07