HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217947Generated: November 2, 2026
1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dione → 3-methoxy-4-(1-ethoxyethoxy)styrene N-(4-hydroxyphenyl)maleimide
https://huagongshe.com/reaction/2217947
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dione | HCID 81734 | — |
| Reactant | HCID 23084984 | HCID 23084984 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-methoxy-4-(1-ethoxyethoxy)styrene N-(4-hydroxyphenyl)maleimide | HCID 86604069 | 88% |
Reaction Steps
In a reaction vessel, 111.14 g (0.5 mol) of 3-methoxy-4-(1-ethoxyethoxy)styrene and 94.59 g (0.5 mol) of N-(4-hydroxyphenyl)maleimide were dissolved in 400 ml of tetrahydrofuran. While stirring the resulting solution, a nitrogen gas was passed into the system. Subsequently, 12.42 g (0.05 mol) of polymerization initiator V-65 (produced by Wako Pure Chemical Industries, Ltd.) was added thereto and the reaction solution was heated at 65° C. After stirring under heat for 10 hours by adding V-65 in the same amount as above every one hour, the reaction solution was allowed to cool to room temperature and then added dropwise in 5 L of hexane to precipitate a polymer. The solid obtained by filtration was dissolved in 800 ml of tetrahydrofuran and the resulting solution was again added dropwise in 5 L of hexane. After filtration, the solid obtained was dried under reduced pressure to obtain 181.04 g of a 3-methoxy-4-(1-ethoxyethoxy)styrene/N-(4-hydroxyphenyl)maleimide copolymer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410747B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-2d9eae9bd16f4795b56e953c5ba9ef37 |
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| Source note | uspto-grants-2008_08 |
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