HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → 1-Ethyl-4-(prop-2-ynyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Ethyl-4-(prop-2-ynyl)piperazine | HCID 21190741 | — |
Reaction Steps
To the 1-ethylpiperazine (2.33 g, 20.2 mmol) and K2CO3 (2.79 g, 20.2 mmol) in acetone (27 ml) was added propargyl bromide (2.00 g, 13.5 mmol) dropwise at 0° C. under N2. The reaction was stirred at room temperature overnight. The reaction was filtered and the salts washed with a small amount of acetone. The filtrates were combined and evaporated gently to concentration. The residue was taken up in EtOAc and washed with water. The aqueous phase was re-extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. The product was filtered and evaporated to dryness to leave a pale orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428439B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-1aecab577c21433f8f76a6b004c2785f |
| Source note | uspto-grants-2016_08 |