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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436156Generated: October 25, 2026

Water → [(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanol

https://huagongshe.com/reaction/1436156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactantmethyl(2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylateHCID 67462967—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product[(2R,6S)-6-(4-chlorophenyl)piperidin-2-yl]methanolHCID 6746019686.5%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Lithium aluminum hydride (508 mg) was suspended in THF (50 mL) in a nitrogen atmosphere. Methyl (2R,6S)-6-(4-chlorophenyl)piperidine-2-carboxylate (2.47 g) was added to the suspension at −20° C., and the reaction solution was stirred at −20° C. for one hour. Water (0.51 ml), a 5 N sodium hydroxide solution (0.51 ml), and water (1.53 ml) were sequentially added to the reaction solution at −20° C., and the reaction solution was stirred at room temperature for 15 minutes. Ethyl acetate was added to the reaction solution. Then, the reaction solution was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: Chromatorex NH; elution solvent: heptane-ethyl acetate system) to obtain 1.90 g of the title compound. The property value of the compound is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618960B2
Source datasetuspto-grants-2009_11
ORD IDord-3cdcfb92dc344b60b25eb750a4f762c8
Source noteuspto-grants-2009_11