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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791636Generated: November 4, 2026

4-Pyridineethanol → 4-Piperidineethanol

https://huagongshe.com/reaction/1791636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridineethanolHCID 72921—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventAcetic AcidHCID 176—
Product4-PiperidineethanolHCID 7395346%

Reaction Steps

A solution of 4-(2-hydroxyethyl)pyridine (1.8 g, 14.6 mol) in acetic acid (15 ml) containing platinum oxide (200 mg) was hydrogenated for 20 hours at 3.3–4 atmospheres pressure. After filtration, the filtrate was evaporated and azeotroped twice with toluene. The residue was triturated with 2N sodium hydroxide and solid sodium hydroxide was added to adjust the pH to 13. The volatiles were removed under vacuum and the residue was triturated with ether, filtered, washed with methylene chloride, and dried under vacuum to give 2-(piperidin-4-yl)-1-ethanol (860 mg, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-96881d55c9224543ab8da979c8651f3b
Source noteuspto-grants-2006_07