HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 4-METHYL-PIPERAZINE-1-CARBONITRILE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Product | 4-METHYL-PIPERAZINE-1-CARBONITRILE | HCID 10419183 | — |
Reaction Steps
In the manner given in Example 1, N-methylpiperazine is treated with cyanogen bromide and aqueous sodium hydroxide to give 4-methyl-1-piperazinecarbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098791 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-60421e53c55e4d9583bbf1b39cf49d92 |
| Source note | uspto-grants-1978_07 |