HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375415Generated: October 28, 2026
Maleic Anhydride → HCID 18995300, compound
https://huagongshe.com/reaction/375415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | HCID 15217322 | HCID 15217322 | — |
| Catalyst | Phosphoric Acid | HCID 1004 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 18995300 | HCID 18995300 | 97.4% |
Reaction Steps
In the same reactor used in Example 2D, there were placed 26.5 g (0.27 mole) of maleic anhydride, 0.7 g of phosphoric acid and 150 ml of mixed xylene. A solution was then added dropwise thereto, the solution having been prepared by thermally dissolving 52.8 g (0.1 mole) of 1,4-bis[4-(3-aminophenoxy)-α,α-dimethylbenzyl]benzene obtained in Example 1D in a mixture of 100 ml of mixed xylene and 50 ml of N,N-dimethylformamide. A dropping time of 5 hours and an aging time of 2 hours were used in order to carry out the reaction. The reaction solution was concentrated to about 1/2 the original amount and then cooled. When a temperature of 80° C. had been reached, 50 g of water was added thereto. Afterward, the solution was slowly cooled, so that crystals precipitated. The precipitated crystals were then cooled to room temperatures filtered; and washed with cold methanol. 67.1 g of desired crude 1,4-bis[4-(3-maleimidophenoxy)-α,α-dimethylbenzyl]benzene was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484948 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-d860950201214c20ada24a18949842dd |
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| Source note | uspto-grants-1996_01 |
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