HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Anhydride → 1,2,3,4-Cyclobutanetetracarboxylic dianhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Catalyst | Mercury | HCID 23931 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,2,3,4-Cyclobutanetetracarboxylic dianhydride | HCID 107280 | 100% |
Reaction Steps
In a 1 liter-glass flask equipped with a 500 W moderate-pressure mercury lamp, 100 g (1.02 M) of maleic anhydride and 1 kg of ethyl acetate were placed and mixed to provide a homogeneous solution. Under stirring in an agron atmosphere, the solution was irradiated with light by using the mercury lamp for 8 hours at 20° C. to precipitate a crystal. After the reaction, the crystal was recovered by filtration to obtain 3.3 g of cyclobutanetetracarboxylic dianhydride (100% trans form).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06001276 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-7e8636e3b437432283c323dab4460fe3 |
| Source note | uspto-grants-1999_12 |