Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Tetramethylammonium hydroxide | HCID 60966 | — |
| Reactant | 3-(Hydroxymethyl)-1H-pyrrole-2,5-dione | HCID 21981751 | — |
| Reactant | Maleimide styrene | HCID 66643759 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Cyclohexanone | HCID 7967 | — |
| Product | Styrene methylol maleimide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810613 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-19bfcb862fad456b9e524e6a7e2e59b0 |
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| Source note | uspto-grants-1989_03 |
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