HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-fluoro-4-nitro-5-carboxyphenyl)-2,3-dimethylmaleic acid imide → N-(2-fluoro-5-carboxy-4-aminophenyl)-2,3-dimethylmaleic acid imide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-fluoro-4-nitro-5-carboxyphenyl)-2,3-dimethylmaleic acid imide | HCID 54493468 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-fluoro-5-carboxy-4-aminophenyl)-2,3-dimethylmaleic acid imide | HCID 17802076 | 92.6% |
Reaction Steps
67.8 g of N-(2-fluoro-5-carboxy-4-nitrophenyl)-2,3-dimethylmaleic acid imide are hydrogenated using hydrogen in the presence of 14 g of Raney nickel catalyst in 1000 ml of tetrahydrofuran at a temperature of 20°-25° under normal pressure. When the stoichiometric amount of hydrogen has been consumed, the catalyst is separated off and the solution is concentrated by evaporation. 56.7 g of N-(2-fluoro-5-carboxy-4-aminophenyl)-2,3-dimethylmaleic acid imide having a melting point of 270° are thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04804400 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-f2e2eea0f93241a6a33c16d935641036 |
| Source note | uspto-grants-1989_02 |