HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 86605409, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | HCID 76498487 | HCID 76498487 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86605409 | HCID 86605409 | 78% |
Reaction Steps
2.0 g of methylmethacryilic acid, 9.0 g of t-butylacrylate, 1.0 g of maleic anhydride, 1.2 g of N-[(perfluorooctanesulfonyl)oxy]-norbornene-2,3-dicarboximide and 0.5 g of AIBN were dissolved in 50 g of acetone. The monomers were polymerized at 67° C. for 6 hours. After completion of the polymerization, the polymerized product was precipitated in water, filtered, and dried in a vacuum to give poly(methylmethacrylic acid-t-butylacrylate-maleic anhydride-N-[(perfluorooctanesulfonyl)oxy]-norbornene-2,3-dicarboximide) in a yield of 78%. The structure of the polymer was identified by 1H-NMR spectroscopy (FIG. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07303858B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-1fd61f07b4db4307a2d06c5efcf64cc1 |
| Source note | uspto-grants-2007_12 |