HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709816Generated: October 26, 2026
Hydrochloric Acid → 4-(Diphenylmethyl)piperidine hydrochloride
https://huagongshe.com/reaction/1709816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Benzhydrylpyridine | HCID 77252 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetonitrile methanol | HCID 21959252 | — |
| Product | 4-(Diphenylmethyl)piperidine hydrochloride | HCID 23004093 | — |
Reaction Steps
A mixture of 62.69 g (0.256 mole) of diphenyl-4-pyridylmethane and 6.4 g of 10% palladium on carbon (0.0060 mole) in 300 ml of glacial acetic acid and under an atmosphere of hydrogen (44 psi) was shaken on a Parr apparatus at 865° for 4 days. The reaction mixture was filtered, and the solvent was removed in vacuo from the filtrate. The residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give a solid. This was dissolved in a mixture of methanol-acetonitrile, and excess ethereal hydrogen chloride was added. A precipitate was collected to give 59.13 g (80.3%) of slightly impure title compound as a white, crystalline solid, m.p. 273°-274° C. Part of this was recrystallized from methanol-ether to give an analytically pure sample, m.p. 275.5°-277° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950674 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-fab04107275b4890aeb9f104e17555f5 |
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| Source note | uspto-grants-1990_08 |
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