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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548625Generated: October 29, 2026

Piperidine → (5S)-5-(piperidin-1-ylmethyl)pyrrolidin-2-one

https://huagongshe.com/reaction/548625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant[(2S)-5-oxopyrrolidin-2-yl]methyl 4-methylbenzene-1-sulfonateHCID 2734055—
SolventAcetonitrileHCID 6342—
Product(5S)-5-(piperidin-1-ylmethyl)pyrrolidin-2-oneHCID 57550249100%

Reaction Steps

Piperidine a14 (0.7 g, 8.3 mmol, 1.5 eq) is added to a suspension of [(2S)-5-oxopyrrolidin-2-yl]methyl 4-methylbenzenesulfonate a13 (1.5 g, 5.56 mmol, 1 eq) and potassium carbonate (1.5 g, 11.1 mmol, 2 eq) in acetonitrile (50 ml), and the mixture is stirred at reflux overnight. Potassium carbonate is filtered and the solvent is removed in vacuo. The residue is dissolved in a minimum of dichloromethane, then the organic layer is sonicated and heated to precipitate a white solid which is filtered. The liquid phase is concentrated in vacuo to give 1 g of (5S)-5-(piperidin-1-ylmethyl)pyrrolidin-2-one a15 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943605B2
Source datasetuspto-grants-2011_05
ORD IDord-274543a02ff94f01b9eb850d1114ab7f
Source noteuspto-grants-2011_05