HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Carbamoyl-1-phenylpyridinium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 4-Carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride | HCID 10616003 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Carbamoyl-1-phenylpyridinium chloride | HCID 10704884 | — |
Reaction Steps
A mixture of 4-carbamoyl-1-(2,4-dinitrophenyl)pyridinium chloride (50 g, prepared in a similar manner to that described in Example 2), aniline (35 ml) and methanol (11) was stirred at ambient temperature for 48 hours. The resulting suspension was heated at 50° C. for 1 hour, then cooled and the solvent removed in vacuo. The solid residue was triturated with acetone (2×11) then collected by filtration to give 4-carbamoyl-1-phenylpyridinium chloride (33.24 g), mp 290°-292° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05767116 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-f647a45feb8b41c5ad0f416ef5c76f45 |
| Source note | uspto-grants-1998_06 |