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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547183Erstellt: 24. Oktober 2026

Water → (R)-(1-methylpiperidin-3-yl)methanol

https://huagongshe.com/de/reaction/547183

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Eduktethyl (3R)-1-methylpiperidine-3-carboxylateHCID 736036—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-(1-methylpiperidin-3-yl)methanolHCID 92011394,3%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A solution of (R)-ethyl 1-methylpiperidine-3-carboxylate (5.69 g, 33 mmol) in ether (20 ml) was added dropwise to a stirred solution of lithium aluminum hydride (36.6 ml of a 1M solution in THF, 36.6 mmol) in ether (85 ml) cooled to maintain a reaction temperature of 20° C. The mixture was stirred for 1.5 hours at ambient temperature and then water (1.4 ml), 15% aqueous sodium hydroxide solution (1.4 ml) and then water (4.3 ml) were added. The insolubles were removed by filtration and the volatiles removed from the filtrate by evaporation to give (R)-(1-methylpiperidin-3-yl)methanol (4.02 g, 94%) as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE042353E1
Quelldatensatzuspto-grants-2011_05
ORD IDord-358144f660614c7e80a93663495202a3
Quellennotizuspto-grants-2011_05