HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019474Generated: October 31, 2026
Azobisisobutyronitrile → HCID 131731368, compound
https://huagongshe.com/reaction/1019474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | HCID 86613229 | HCID 86613229 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131731368 | HCID 131731368 | 75.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08715900B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-7d910bea30ed47aaa3f79b2c6d925c26 |
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| Source note | uspto-grants-2014_05 |
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