HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → N-Methylphthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 2-methyl-5-phenoxyisoindole-1,3-dione | HCID 821556 | — |
| Product | N-Methylphthalimide | HCID 11074 | 46% |
Reaction Steps
The above results show that an exchange occurred between 4-phenoxy-N-methylphthalimide and phthalic anhydride, resulting in a 46% yield of N-methylphthalimide and a 64% yield of 4-phenoxyphthalic anhydride or acid. This conversion of 4-phenoxy-N-methylphthalimide to 4-phenoxyphthalic anhydride was achieved in a direct manner without any requirement for converting the 4-phenoxy-N-methylphthalimide to the corresponding hydrazide or the base hydrolysis thereof, resulting in the production of metal salt requiring the neutralization and heating of the resulting phthalic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217281 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-796184338a7c4165a53017e35c02ff7c |
| Source note | uspto-grants-1980_08 |