Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methacrylamide | HCID 6595 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Cyclohexyl methacrylate | HCID 7561 | — |
| Product | Methacrylamide | HCID 6595 | — |
| Product | Styrene | HCID 7501 | — |
| Product | Cyclohexyl methacrylate | HCID 7561 | — |
| Product | 3,5-Dimethylpiperidine-2,6-dione | HCID 264790 | — |
Reaction Steps
A 2,4-dimethylglutarimide, styrene, and cyclohexyl methacrylate containing polymer was prepared by the techniques of copolymerization and glutarimidization. Accordingly an interpolymer of styrene, cyclohexyl methacrylate, and methacrylamide was prepared. In a 1.5 liter, glass reactor fitted with inlet tubes, nitrogen pad, and stirrer, styrene 29 g, cyclohexyl methacrylate 225 g, and methacrylamide 122 g, were introduced, along with 50 percent based o monomer weight of N,N-dimethylformamide solvent. 250 ppm of a peroxide initiator 1,1-bis(t-butylperoxy)cyclohexane was introduced and the reactor heated to 80-100° C. with stirring. Reaction was continued only a short time period (10-20 percent conversion) to prevent polymer compositional drift and possible degeneration of optical properties. The polymer was recovered by precipitation in methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05218068 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-16767af77c4f400e8ffc23813fb49c22 |
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| Source note | uspto-grants-1993_06 |
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