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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268133Generated: October 30, 2026

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

https://huagongshe.com/reaction/2268133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMagnesium ChlorideHCID 5360315—
Reactant(+)-4-(4-Fluorophenyl)-1,2,3,6-tetrahydro-1-(phenylmethyl)-3-pyridinemethanolHCID 9912522—
ReactantHCID 21862873HCID 21862873—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttrans 1-Benzyl-4-(4-fluorophenyl)-3-piperidinemethanolHCID 1088110181.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium 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) in THF (1.7 ml) was added dropwise over approximately 2 minutes. The reaction mixture was stirred and boiled under reflux for 4 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 using the conditions described above. Starting material 13.2% was still present in the product as analysed by GLC. The amount of desfluoro compound as determined by HPLC was less than 0.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326496B1
Source datasetuspto-grants-2001_12
ORD IDord-3e5b2d865d2647a0acc1b15ba4c76e55
Source noteuspto-grants-2001_12