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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838547Generated: October 25, 2026

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

https://huagongshe.com/reaction/1838547

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 aluminium 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 colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673803B2
Source datasetuspto-grants-2004_01
ORD IDord-9826ab7524ff42069f3a17275785d56a
Source noteuspto-grants-2004_01