HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → N-Phenyltetrachlorophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Tetrachlorophthalic anhydride | HCID 8326 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-Phenyltetrachlorophthalimide | HCID 319375 | — |
Reaction Steps
In a preferred embodiment tetrachlorophthalic anhydride is refluxed with aniline in the presence of glacial acetic acid for 5 to 10 hours to form tetrachloro-N-phenylphthalimide which is reacted with KF in sulfolane in the presence of tributylhexadecylophosphonium bromide under nitrogen at 140° C. to 160° C. for 10 to 15 hours to form tetrafluoro-N-phenylphthalimide which in turn is hydrolyzed by refluxing with 50% H2SO4 for 15 to 25 hours. The tetrafluoro-N-phenylphthalimide is a novel compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05047553 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-0c80dbaab8fa4a0d9a59256abf011562 |
| Source note | uspto-grants-1991_09 |