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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955218Generated: November 2, 2026

Diethyl Ether → HCID 6918426, compound

https://huagongshe.com/reaction/1955218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-Benzyl-4-(4-methylbenzyl)piperidin-4-olHCID 10592641—
Reactant4-[(4-Methylphenyl)methyl]piperidin-4-ol hydrochlorideHCID 22628376—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 6918426HCID 691842692%

Reaction Steps

4-Hydroxy-4-(4-methylbenzyl)piperidine hydrochloride. A mixture of 1-benzyl-4-(4-methylbenzyl)-4-hydroxypiperidine (2.8 g, 9.5 mmol) and 700 mg of 10% Pd/C in 100 mL of 95% ethanol was hydrogenated at 50 psi for overnight. The catalyst was removed through a short column of celite (10 g) and washed with methanol (3×15 mL). To the filtrate was added 12 mL of 1M HCl in methanol. Evaporation of methanol gave a residue, to which was added 30 mL of ether. The mixture was stirred at rt for 2 days. A white solid was collected by filtration, giving 2.1 g (92%) of the title product. mp 183-185° C. 1H NMR (CDCl3) 1.680 (m, 2 H), 2.097 (m, 2 H), 2.338 (s, 3 H), 2.783 (s, 2 H), 3.241 (m, 5 H), 7.049 (d, J=7.5 Hz, 2 H), 7.142 (d, J=7.5 Hz, 2 H), 9.30 (brs, 1 H), 9.515 (brs, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124323
Source datasetuspto-grants-2000_09
ORD IDord-1999d381c970477ea6f7f857c4928f35
Source noteuspto-grants-2000_09