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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268132Generated: November 1, 2026

Sodium Hydroxide → trans 1-Benzyl-4-(4-fluorophenyl)-3-piperidinemethanol

https://huagongshe.com/reaction/2268132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMagnesium ChlorideHCID 5360315—
Reactant(+)-4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-(phenylmethyl)-3-pyridinemethanolHCID 9912522—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttrans 1-Benzyl-4-(4-fluorophenyl)-3-piperidinemethanolHCID 1088110181.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Lithium aluminium hydride in THF (2.0 ml of a 1M solution) was carefully added to substantially anhydrous magnesium chloride (0.19 g, 1.5% H2O) under nitrogen. The mixture was stirred and heated to 50° C. and then a solution of (+)-1-benzyl-3-hydroxymethyl-4-(4-fluorophenyl)-1,2,3,6-tetrahydropyridine (0.60 g, preparation given in WO96136636) in THF (1.7 ml) was added dropwise over approximately 2 minutes. The reaction mixture was stirred and boiled under reflux for 4.2 hours. The mixture was cooled to ambient temperature and then stirred in an ice/water bath whilst water (0.1 ml) then 5M sodium hydroxide solution (0.1 ml) and water (0.1 ml) were added. The suspension was diluted with THF (5 ml) and the mixture filtered. The residue was washed with THF (3×5 ml) and the combined filtrate and washings were evaporated under reduced pressure to give a yellow oil (0.49 g). This oil was analysed by GLC, Chiral HPLC and 1H nmr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326496B1
Source datasetuspto-grants-2001_12
ORD IDord-8cac6582eb4d41a5a5c8e8a097d34b83
Source noteuspto-grants-2001_12