Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547182Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/547182

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
PatentnummerUSRE042353E1
Quelldatensatzuspto-grants-2011_05
ORD IDord-c68b3b5ec2e34710853692c235db63a0
Quellennotizuspto-grants-2011_05