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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174696Generated: October 30, 2026

Ethyl Acetate → HCID 66584436, compound

https://huagongshe.com/reaction/2174696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86660670HCID 86660670—
SolventAcetonitrileHCID 6342—
ProductHCID 66584436HCID 66584436—

Reaction Conditions

Temperature80 °C

Reaction Steps

The 4-tosyloxypropyl-N-(4-nitrophenyl)piperidine (4.19 g, 10.0 mmol) obtained in Example 11(2) was dissolved in acetonitrile (40 ml), and potassium carbonate (2.76 g, 20 mmol) and 1,2,4-triazole (1.04 g, 15.0 mmol) were added thereto, followed by stirring at 80° C. for 18 hours. After the reaction mixture was allowed to cool to room temperature, ethyl acetate was added to the reaction mixture, and the organic layer was washed with water and saturated sodium chloride, and dried over anhydrous sodium sulfate. After the desiccant was filtered off, the residue obtained by evaporation under reduced pressure was purified using medium pressure silica gel flash column chromatography (methanol:chloroform=1:100 to 1:30), thereby obtaining 4-[3-(1,2,4-triazol-1-yl)-propyl]-N-(4-nitrophenyl)piperidine (2.47 g, 78%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062035B2
Source datasetuspto-grants-2015_06
ORD IDord-2d730b9e940b467f8c85dc011feae8d7
Source noteuspto-grants-2015_06