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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088430Generated: October 28, 2026

Ammonia → Styrene methylol maleimide

https://huagongshe.com/reaction/1088430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantStyreneHCID 7501—
ReactantTetramethylammonium hydroxideHCID 60966—
Reactant3-(Hydroxymethyl)-1H-pyrrole-2,5-dioneHCID 21981751—
ReactantMaleimide styreneHCID 66643759—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventCyclohexanoneHCID 7967—
ProductStyrene methylol maleimideHCID 86742784—

Reaction Steps

Styrene methylol maleimide copolymer was prepared by copolymerizing styrene (0.9 g) with methylol maleimide (1.0 g) in 10 ml cyclohexanone at 70° C. using azobisisobutylronitrile as an initiator for a period of 3 hours. The polymer was isolated by trituration of the solid, cooled reaction mixture with methanol. A sample of the polymer was examined by 1H/NMR (proton nuclear magnetic resonance) and found to have a spectrum consistent with the assigned composition. An IR spectrum of a film prepared from DMF solution showed a band in the region where OH stretching is expected. The polymer was found to be insoluble in water, but soluble in dilute tetramethyl ammonium hydroxide solution. A film treated with ammonia vapor gave an IR spectrum which no longer had the band associated with the --CH2OH group but which conformed to the spectrum of maleimide styrene copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04962171
Source datasetuspto-grants-1990_10
ORD IDord-6afc3342cc9d44ee9579a43b0a5c209e
Source noteuspto-grants-1990_10