HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 3-Methylbenzylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | m-Xylyl bromide | HCID 12099 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Methylbenzylpiperazine | HCID 79213 | 78.1% |
Reaction Steps
α-Bromo-m-xylene (10 ml, 74 mmole) was added to a solution of 75 g (11.8 equiv.) of anhydrous piperazine in 500 ml of benzene and the reaction was heated to reflux for two hours. After cooling to room temperature, the reaction was diluted with 300 ml of diethyl ether and washed with 500 ml of 0.2 M sodium hydroxide followed by two 500 ml portions of water. The organic solution was dried over sodium sulfate and the solvent removed to give 11.0 g (78%) of crude 1-(3-methylbenzyl)piperazine as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05124330 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-c6e0b8d02e2348fcb55532b1fe88386d |
| Source note | uspto-grants-1992_06 |