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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1791534Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1791534

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormic AcidHCID 284—
EduktSodium HydroxideHCID 14798—
Eduktethyl (3R)-piperidine-3-carboxylateHCID 185582—
EduktSodium BicarbonateHCID 516892—
LösungsmittelFormaldehydeHCID 712—
Produktethyl (3R)-1-methylpiperidine-3-carboxylateHCID 73603673%

Reaktionsschritte

(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07074800B1
Quelldatensatzuspto-grants-2006_07
ORD IDord-a0c6379d14634e24819afeaf203f941c
Quellennotizuspto-grants-2006_07