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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227931Generated: November 2, 2026

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

https://huagongshe.com/reaction/2227931

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 numberUS06414148B1
Source datasetuspto-grants-2002_07
ORD IDord-daa39509b0934e7a85bcca48b7146551
Source noteuspto-grants-2002_07