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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380463Generated: November 3, 2026

4-Phenyl-1,2,3,4-tetrahydropyridine--hydrogen chloride (1/1) → 4-Phenylpiperidine

https://huagongshe.com/reaction/380463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenyl-1,2,3,4-tetrahydropyridine--hydrogen chloride (1/1)HCID 22475067—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-PhenylpiperidineHCID 6987359.1%

Reaction Steps

A mixture of 20.5 g (104.9 mmol) of 4-phenyltetrahydropyridine hydrochloride (Aldrich) and 0.5 g of 10% Pd/C in 40 mL of H2O and 160 mL of EtOH was stirred under hydrogen at 45 psi for 2 h. The reaction mixture was then filtered though a thin pad of celite eluting with EtOH and H2O. The filtrate was concentrated and the residue was stirred in 75 mL of ether. To it at 0° C. was added 5 g of solid NaOH. The layers were separated and the aqueous layer was extracted with ether. The combined organic fractions were washed with sat'd NaCl solution, dried over Na2SO4, filtered and the filtrate was concentrated. The residue was crystalized from cold heptane to give 10 g of the title compound. 1H NMR (CDCl3) δ7.33 (t, 2H, J=7.7 Hz), 7.25-7.28 (m, 3H), 6.90 (bs, 1H), 3.65 (d, 2H, J=12.6 Hz), 3.04 (d of d,2H, J=13.0, 2.5 hz), 2.78 (t of d, 1H, J=12.1, 3.2 Hz), 2.21-2.30 (m,2H), 2.05 (d, 2H, J=14.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303593B1
Source datasetuspto-grants-2001_10
ORD IDord-79764fbe273149d0984164fe30601166
Source noteuspto-grants-2001_10