HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1-Allylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trifluoroacetylpiperazine | HCID 7172020 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Allylpiperazine | HCID 806422 | 155.1% |
Reaction Steps
To a stirred solution of 2,2,2-trifluoro-1-piperazin-1-yl-ethanone (515 mg, 2.83 mmol) in dry CH3CN (6 mL) was added allyl bromide (0.32 mL, 3.7 mmol) and powdered potassium carbonate (0.78 g, 5.65 mmol) and the mixture stirred overnight. The reaction was concentrated under reduced pressure, diluted with CH2Cl2 (30 mL) and water (30 mL) and the aqueous layer extracted with CH2Cl2 (2×20 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo to afford the crude di-protected piperazine (0.554 g) which was used without further purification in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091217B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-32ee4c940d754b23bf862be162c61ba9 |
| Source note | uspto-grants-2006_08 |