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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207773Generated: October 31, 2026

Triethylamine → 1-(2-quinolinyl)-4-Piperidinol

https://huagongshe.com/reaction/2207773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChloroquinolineHCID 11928—
ReactantPiperidin-4-olHCID 79341—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(2-quinolinyl)-4-PiperidinolHCID 4051641860%

Reaction Conditions

Temperature100 °C

Reaction Steps

Triethylamine (2.9 g, 29.6 mmol), 2-chloro-quinoline (purchased from Alfa Aesar™) (2.4 g, 14.8 mmol) and piperidin-4-ol (1.5 g, 14.8 mmol) were dissolved in DMF (20 mL). The resulting mixture was heated to 100° C. overnight. The mixture was then diluted with water (20 mL) and extracted with EtOAc (2×50 mL). The combined organic extracts were combined and washed with water (20 mL) and brine (20 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 70% EtOAc in petroleum ether) to give 1-(quinolin-2-yl)piperidin-4-ol (2.0 g, 8.7 mmol, 60% yield) as white solid. ESI-MS (M+1): 229 calc. for C14H16N2O 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-2e44f31cc2db4c10b359e075d7c5032f
Source noteuspto-grants-2016_06