Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204936Generated: November 1, 2026

Azobisisobutyronitrile → HCID 131731368, compound

https://huagongshe.com/reaction/2204936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
ReactantHCID 86613229HCID 86613229—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131731368HCID 13173136875.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

Maleic Anhydride (MA, 7.4 g, 75.0 mmol), Phenyl Ethyl Norbornene (PENB, 14.9 g, 75.0 mmol) and AIBN (1.2 g, 7.5 mmol) was dissolved in THF (32.1 g) and charged to an appropriately sized reaction vessel. The solution was sparged with nitrogen for 10 min to remove oxygen and then heated to 70° C. The mixture was allowed to stir at 70° C. for 17.5 hr, after which the solution was cooled to room temperature. The reaction mixture was diluted with 30 g of THF and added to hexane (1 L) to give a white powder that was filtered and dried in a vacuum oven at 80° C. for 16 hr. Approximately, 16.7 g (75%) of the MA/PENB polymer was isolated (GPC Mw=3,400 Mn=1,500).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09366956B2
Source datasetuspto-grants-2016_06
ORD IDord-f584f53b39c24f6c988255bf8035a878
Source noteuspto-grants-2016_06