HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-[(4-Bromophenyl)methyl]piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-[(4-Bromophenyl)methyl]piperazine | HCID 876494 | — |
Reaction Steps
This compound could be made in the following manner: 2 g of 4-Bromobenzyl bromide and 1 equ. piperazine in acetonitrile would be stirred at room temperature and 1.1 g of potassium carbonate would be added. The reaction would be stirred at room temperature overnight. The solution would then be filtered through Celite and concentrated in vacuo to afford the crude product. Purification would be done by flash chromatography using a methylene chloride/methanol gradient.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595397B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-644b95f8f0c442a188f83b3f6390af57 |
| Source note | uspto-grants-2009_09 |