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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Phenyl-1,2,3,4-tetrahydropyridine--hydrogen chloride (1/1) | HCID 22475067 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Phenylpiperidine | HCID 69873 | 59.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303593B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-79764fbe273149d0984164fe30601166 |
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| Source note | uspto-grants-2001_10 |
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