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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12760119HCID 12760119—
ReactantHCID 14593334HCID 14593334—
ReactantHCID 18695554HCID 18695554—
CatalystPalladiumHCID 23938—
CatalystCopperHCID 23978—
SolventSulfolaneHCID 31347—
Product4-Acetamido-1-[6-(2,2,2-trifluoro) ethoxy-2-pyridyl]piperidineHCID 12926619—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409228
Source datasetuspto-grants-1983_10
ORD IDord-abc52f84b510419bb52e0236742574fe
Source noteuspto-grants-1983_10