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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dioneHCID 81734—
ReactantHCID 23084984HCID 23084984—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-methoxy-4-(1-ethoxyethoxy)styrene N-(4-hydroxyphenyl)maleimideHCID 8660406988%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410747B2
Source datasetuspto-grants-2008_08
ORD IDord-2d9eae9bd16f4795b56e953c5ba9ef37
Source noteuspto-grants-2008_08