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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722810Generated: November 2, 2026

Azobisisobutyronitrile → HCID 86743294, compound

https://huagongshe.com/reaction/1722810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantCyclohexanoneHCID 7967—
ReactantMaleimideHCID 10935—
Reactant4-tert-ButylstyreneHCID 15627—
SolventWaterHCID 962—
ProductHCID 86743294HCID 8674329495%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857435
Source datasetuspto-grants-1989_08
ORD IDord-3c1c817b7c4b4bfb9dc2ec688a467a29
Source noteuspto-grants-1989_08