HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 4-Methylpiperidine-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Reactant | Disodium hydroxide | HCID 21696466 | — |
| Product | 4-Methylpiperidine-1-carbonitrile | HCID 13442629 | — |
Reaction Steps
In the manner given in Example 1, 4-methylpiperidine is treated with cyanogen bromide and aqueous sodium sodium hydroxide to give 4-methyl-1-piperidinecarbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04098791 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-50cf9d99c70047a18b3a7db36c76f152 |
| Source note | uspto-grants-1978_07 |