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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278520Generated: October 31, 2026

Water → (-)-trans-4-(4'-Fluorophenyl)-3-hydroxymethyl-N-methylpiperidine

https://huagongshe.com/reaction/1278520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantLithium ChlorideHCID 433294—
Reactanttrans-3-Ethoxycarbonyl-4-(4'-fluorophenyl)-1-methylpiperidine-2,6-dioneHCID 15405466—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product(-)-trans-4-(4'-Fluorophenyl)-3-hydroxymethyl-N-methylpiperidineHCID 2734218—

Reaction Steps

To a cooled mixture of NaAlH4 (0.22 mol) in toluene is added LiCl (0.11 mol) in THF. Note: LiCl can be added to the reactor prior to the addition of NaAlH4 or after the addition of the substrate, (+/−)trans 3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione. Next, (+/−)trans 3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione (0.083 mol) is added in THF (65 ml) holding the temperature below 15° C. After addition is completed, reaction is allowed to warm to room temperature. After 30 minutes at room temperature, the reaction is heated to >40° C. for 2 hr. The reaction is then cooled to <5° C. and toluene (50 ml) is added. Water (9 ml) is then added slowly holding the temperature below 15° C. Additional H2O or aqueous NaOH is used as necessary. The solid inorganic salts are removed by filtration. These solids are washed with additional THF or toluene. The filtered solution is then concentrated to give (+/−) trans-4-(4′-fluorophenyl)-3-hydroxymethyl-N-methylpiperidine in essentially the same yield and similar impurity profile as with LiAlH4 as shown by HPLC analysis. The product can be recovered by standard procedures such as trituration with a less polar solvents.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444190B2
Source datasetuspto-grants-2002_09
ORD IDord-10b6824bcbc0490f9bb5c5e5887e5132
Source noteuspto-grants-2002_09