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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278519Generated: November 1, 2026

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

https://huagongshe.com/reaction/1278519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
Reactanttrans-3-Ethoxycarbonyl-4-(4'-fluorophenyl)-1-methylpiperidine-2,6-dioneHCID 15405466—
SolventTetrahydrofuranHCID 8028—
SolventTetrahydrofuran tolueneHCID 22635083—
Product(-)-trans-4-(4'-Fluorophenyl)-3-hydroxymethyl-N-methylpiperidineHCID 2734218—

Reaction Steps

To a cooled 50:50 mole mixture of NaAlH4/LiAlH4 (0.22 mol) in toluene/THF under argon is added (+/−) trans-3-ethoxycarbonyl-4-(4′-fluorophenyl)-N-methyl-piperidine-2,6-dione (0.083 mol) in THF holding the temperature below 15° C. After addition is complete, the reaction is allowed to warm to room temperature. After 30 minutes at room temperature reaction is heated to >40° C. for 2 hr. 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-8f1d3daf16334d058f3f2e5078148b13
Source noteuspto-grants-2002_09