HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium sulfate decahydrate → (2S)-2-(tetrahydro-2H-pyran-4-ylmethyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | (3S)-3-(tetrahydro-2H-pyran-4-ylmethyl)-2,5-piperazinedione | HCID 66582474 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-2-(tetrahydro-2H-pyran-4-ylmethyl)piperazine | HCID 66582396 | 76.1% |
Reaction Steps
A 250-mL round-bottomed flask was charged with (3S)-3-(tetrahydro-2H-pyran-4-ylmethyl)-2,5-piperazinedione (1.44 g, 6.78 mmol), 50 mL of THF, and LAH (1M in THF, 27.1 mL, 27.1 mmol, Sigma-Aldrich, St. Louis, Mo.). After heating at reflux for 2 h, the mixture was allowed to cool to room temperature. Sodium sulfate decahydrate (10 g) was then added and the mixture was stirred at temperature for 1 h. The mixture was filtered and the filtrate was concentrated to give (2S)-2-(tetrahydro-2H-pyran-4-ylmethyl)piperazine (0.950 g, 5.16 mmol) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431563B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-2551b4ab4ac847b88ce08d421ff06ded |
| Source note | uspto-grants-2013_04 |