HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanopyridine → N-(4-cyanophenacyl) 4-chloropyridinium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | 4-Chloropyridine | HCID 12288 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Reactant | Benzonitrile, 4-(chloroacetyl)- | HCID 142493 | — |
| Product | N-(4-cyanophenacyl) 4-chloropyridinium chloride | HCID 86734539 | — |
Reaction Steps
Employing the procedure of Example II but replacing 4-chlorophenacyl bromide with a substantially equimolecular amount of 4-cyanophenacyl chloride and replacing 4-cyanopyridine with a substantially equimolecular amount of 4-chloropyridine there is obtained N-(4-cyanophenacyl) 4-chloropyridinium chloride, a solid soluble in water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE029153 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-61207c3156034bb9bc1506a718b848fc |
| Source note | uspto-grants-1977_03 |