HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66396Generated: October 26, 2026
4-Nitrophthalic acid anhydride → 4-Aminophthalic anhydride
https://huagongshe.com/reaction/66396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophthalic acid anhydride | HCID 230976 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Aminophthalic anhydride | HCID 13814390 | 52.7% |
Reaction Steps
In 200 ml of dry ethyl ether, (C2H5)2O, was dissolved 1.93 g of 4-nitrophthalic anhydride (~ 1% solution) to which was added 0.10 g of 5% palladium-on-charcoal and the mixture hydrogenated in a Paar hydrogenator at 39 psi at room temperature, until no more hydrogen was consumed. The catalyst was removed by filtration and the ether removed from the filtrate, maintained at 0° to -5° C, under vacuo, yielding a yellow crystalline solid mixed with non-crystalline viscous mass. When a small sample of this mixture was placed on a metal plate heated to 245° C, the product melted and polymerized immediately to a tough polymer. Extraction of the crystalline-non-crystalline mixture with ether left 0.46 g of polymer; concentration of the ether followed by cooling, yielded 0.86 g of 4-aminophthalic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04131730 |
|---|
| Source dataset | uspto-grants-1978_12 |
|---|
| ORD ID | ord-38965d72a83f4820b52f1ccaccc9bcdb |
|---|
| Source note | uspto-grants-1978_12 |
|---|