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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325688Generated: October 30, 2026

3-Hydroxybenzaldehyde → 1-(3-Hydroxybenzyl)piperidine

https://huagongshe.com/reaction/325688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPiperidineHCID 8082—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(3-Hydroxybenzyl)piperidineHCID 826974—

Reaction Steps

3-Hydroxybenzaldehyde (15 g) and piperidine (15 ml) in ethanol (500 ml) were hydrogenated over 10% palladium/carbon catalyst. The catalyst was removed by filtration and the solvent was evaporated off. The residue was triturated with light petroleum (b.p. 60°-80°) and the resulting solid was recrystallised from acetonitrile to give the title compound as a buff coloured solid (8.7 g) m.p. 134°-7°. TLC silica, methanol, Rf 0.56.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442110
Source datasetuspto-grants-1984_04
ORD IDord-cbbd7bf905644c86be863064567b8d04
Source noteuspto-grants-1984_04