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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427708Generated: October 25, 2026

Triethylamine → 1-(Pyridin-4-yl)piperidin-4-ol

https://huagongshe.com/reaction/427708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BromopyridineHCID 14268—
ReactantPiperidin-4-olHCID 79341—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(Pyridin-4-yl)piperidin-4-olHCID 2344761953.2%

Reaction Steps

A solution of 4-hydroxypiperidine (7.80 g, 77 mmol), 4-bromopyridine (15.0 g, 77 mmol), and triethylamine (32 mL, 231 mmol) in 90 mL of EtOH and 30 mL of H2O was heated at 150° C. in a sealed tube for 4 days. The mixture was concentrated and the residue partitioned between CH2C2 and H2O. The organic layer was washed with 1 N NaOH (2×), diluted with EtOAc and the resulting solid collected by filtration affording 7.30 g (53%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-d997f4cd8a164a31aafd5d785190a383
Source noteuspto-grants-2001_11