HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345915Generated: October 30, 2026
Azobisisobutyronitrile → HCID 86743294, compound
https://huagongshe.com/reaction/345915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Maleimide | HCID 10935 | — |
| Reactant | 4-tert-Butylstyrene | HCID 15627 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86743294 | HCID 86743294 | 95% |
Reaction Steps
Thus, 4 g of maleimide, 6.6 g of 4-(2-methyl-2-propyl) styrene (obtained from Polysciences, Inc.), 42 mg of azobisisobutyronitrile and 40 mL of cyclohexanone were mixed and deoxygenated with argon. This solution was heated in a sealed tube at 60° C. for 4 hours. The resulting polymer was isolated by pouring the polymer solution into cold water, filtering, washing and drying under vacuum. The dried polymer (yield 95% of theoretical) had a melting point of greater than 300° C. The 1H NMR spectrum showed 0.7 NH groups for each aryl group. The polymer was soluble in aqueous alkaline solution of pH equal to 13 or higher. The relative viscosity, ηrel, was 1.15 (0.5 g of polymer per deciliter in DMF at 25° C.). As in Example 2 above, a chain transfer agent may be included to control molecular weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05059513 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-df3f7fa0886349a2b9ba6de8f7976a76 |
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| Source note | uspto-grants-1991_10 |
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