HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → (5S)-5-(piperidin-1-ylmethyl)pyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [(2S)-5-oxopyrrolidin-2-yl]methyl 4-methylbenzene-1-sulfonate | HCID 2734055 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (5S)-5-(piperidin-1-ylmethyl)pyrrolidin-2-one | HCID 57550249 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943605B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-274543a02ff94f01b9eb850d1114ab7f |
| Source note | uspto-grants-2011_05 |