HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane;tetrahydrofuran → (S)-2-Benzylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | Cyclo(-Gly-Phe) | HCID 7076549 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-Benzylpiperazine | HCID 20760001 | 40.3% |
Reaction Steps
To a suspension of (S)-3-benzyl-2,5-dioxopiperazine (2.284 g, 11.18 mmol) in tetrahydrofuran (20 mL) was added borane-tetrahydrofuran complex (49 mL, 1.0 M solution in THF, 49 mmol) at room temperature. The resulting mixture was refluxed for several hours before it was quenched with methanol at 0° C. After concentration in vacuo, the residue was treated with 10% sodium hydroxide aqueous solution, which was extracted with dichloromethane thoroughly. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo to afford white crystals, which were washed with ether to yield (S)-2-benzylpiperazine (795 mg, 40.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504411B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-f1d429434cc449ce9006358226a97478 |
| Source note | uspto-grants-2009_03 |