HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4,5-Dianilinophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | dimethyl 4,5-dianilinobenzene-1,2-dicarboxylate | HCID 10407176 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 4,5-Dianilinophthalimide | HCID 1697 | — |
Reaction Steps
A suspension of 230 mg (0.7 mmol) of 4,5-bis(anilino)phthalic acid dimethyl ester in 23 ml of ethylene glycol is heated at 120°; ammonia gas is passed through the suspension, with stirring, for 24 hours. The reaction mixture is cooled and extracted with ethyl acetate. The ethyl acetate phases are washed in succession three times with water and once with saturated sodium chloride solution, dried with sodium sulfate and concentrated by evaporation. The evaporation residue is chromatographed on silica gel with dichloromethane/methanol 40:1 and the product fractions are combined and concentrated by evaporation, yielding the title compound in the form of yellow crystals, m.p. 215°-217°, FAB-MS: 330 [M+ +H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663336 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-be7c3ef965444e36ba33b12925829af8 |
| Source note | uspto-grants-1997_09 |