HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → (2S,5R)-1-Benzyl-2,5-dimethylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 2,5-Dimethylpiperazine, trans- | HCID 220672 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2S,5R)-1-Benzyl-2,5-dimethylpiperazine | HCID 23402345 | — |
Reaction Steps
50 g trans-2,5 dimethylpiperazine was dissolved in 300 mL ethanol and treated with 26.36 mL (1/2 equivalents) benzylbromide. The mixture was stirred at room temperature for 12 hours and concentrated. The residue was taken up in ethyl acetate and washed with 10% aqueous sodium bicarbonate and saturated sodium chloride; dried over anhydrous magnesium sulfate and concentrated to give crude 1-benzyl-trans-2,5-dimethylpiperazine, as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867209B1 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-29ff725788c848f280bb07ab0401ed6b |
| Source note | uspto-grants-2005_03 |