HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454877Generated: October 29, 2026
Triethylamine → 1-(2-quinolinyl)-4-Piperidinol
https://huagongshe.com/reaction/454877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2-quinolinyl)-4-Piperidinol | HCID 40516418 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-bdbffc3697694aa0b891d087113e87db |
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| Source note | uspto-grants-2013_07 |
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