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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019474Generated: October 31, 2026

Azobisisobutyronitrile → HCID 131731368, compound

https://huagongshe.com/reaction/1019474

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 numberUS08715900B2
Source datasetuspto-grants-2014_05
ORD IDord-7d910bea30ed47aaa3f79b2c6d925c26
Source noteuspto-grants-2014_05