HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647513Generated: October 29, 2026
Potassium Carbonate → 4-Acetamido-1-[6-(2,2,2-trifluoro) ethoxy-2-pyridyl]piperidine
https://huagongshe.com/reaction/647513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12760119 | HCID 12760119 | — |
| Reactant | HCID 14593334 | HCID 14593334 | — |
| Reactant | HCID 18695554 | HCID 18695554 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Sulfolane | HCID 31347 | — |
| Product | 4-Acetamido-1-[6-(2,2,2-trifluoro) ethoxy-2-pyridyl]piperidine | HCID 12926619 | — |
Reaction Steps
A mixture of 19 g of 2-chloro-6-(2,2,2-trifluoroethoxy)pyridine (b.p. 80° C./16 mm Hg, prepared by reaction of 2,6-dichloropyridine with 2,2,2-trifluoroethanolate of sodium), 14.87 g of 4-formamidopiperidine (m.p. 116° to 118° C., prepared by hydrogenation of 4-formamido-1-benzylpiperidine in the presence of palladium on charcoal), 17.27 g of anhydrous potassium carbonate, 5.67 g of copper in powder form in 110 ml of sulfolane is heated to 100° C. with stirring for 50 hours, then the sulfolane is distilled, the residue is taken up with water and the suspension thus obtained is extracted with methylene chloride. The organic phase is washed with water, it is dried over anhydrous sodium sulfate and evaporated to dryness. The residue, firstly crystallised in an 84/16 by volume mixture of water/ethanol and afterwards in diisopropylic ether, gives 9 g of 4-acetamido-1-[6-(2,2,2-trifluoro)ethoxy-2-pyridyl] piperidine; m.p. 92° to 95° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409228 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-abc52f84b510419bb52e0236742574fe |
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| Source note | uspto-grants-1983_10 |
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