HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-(2-Pyrimidinyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Pyrimidinyl)piperazine | HCID 88747 | — |
Reaction Steps
To a solution of anhydrous piperazine (95 g; 1 mol) in ethanol (475 ml), there was added 2-chloropyrimidine (22.9 g; 0.2 mol), and the resultant mixture was stirred at room temperature for 3 hours. After completion of the reaction, a 5% aqueous sodium hydroxide solution was added, followed by extraction with chloroform. The chloroform layer was washed thrice with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was distilled to give 1-(2-pyrimidinyl)piperazine. B.P., 131°-132° C./1.5 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04598078 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-daa0e5c6fd8e4d2a805f7dd5e08c501c |
| Source note | uspto-grants-1986_07 |