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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547183Generated: October 25, 2026

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

https://huagongshe.com/reaction/547183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactantethyl (3R)-1-methylpiperidine-3-carboxylateHCID 736036—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(R)-(1-methylpiperidin-3-yl)methanolHCID 92011394.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042353E1
Source datasetuspto-grants-2011_05
ORD IDord-358144f660614c7e80a93663495202a3
Source noteuspto-grants-2011_05