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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079399Generated: November 2, 2026

Ethyl Acetate → 1-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochloride

https://huagongshe.com/reaction/1079399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-Acetyl-4-piperidoneHCID 122563—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(3-Aminophenyl)piperidine dihydrochlorideHCID 23366944—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-Acetyl-4-[3-(piperidin-1-yl)phenylamino]-piperidine dihydrochlorideHCID 23366900132.1%

Reaction Steps

To a solution of N-(3-aminophenyl)piperidine dihydrochloride (3.73 g) and 1-acetyl-4-piperidone (2.1 g) in methanol (30 ml) was added sodium cyano borohydride (1.9 g), followed by stirring at room temperature for 5 hours. To the mixture were added ethyl acetate ester (20 ml) and water (30 ml), the organic layer was dried over anhydrous sodium sulfate and then the solvent was distilled off. The residual oily compound was separated and purified by silica gel column chromatography (developing solvent: ethyl acetate ester). The oily compound was dissolved in dioxane (10 ml) and to the mixture was added 6N solution of hydrogen chloride in dioxane (2 ml). Then, the solvent was removed to obtain a colorless amorphous solid (3.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580883
Source datasetuspto-grants-1996_12
ORD IDord-3f0c13b8f65045b798b39ce173b37ba1
Source noteuspto-grants-1996_12