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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968462Generated: October 29, 2026

Azobisisobutyronitrile → HCID 86605409, compound

https://huagongshe.com/reaction/968462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantMaleic AnhydrideHCID 7923—
Reactanttert-Butyl acrylateHCID 15458—
ReactantHCID 76498487HCID 76498487—
SolventAcetoneHCID 180—
ProductHCID 86605409HCID 8660540978%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07303858B2
Source datasetuspto-grants-2007_12
ORD IDord-1fd61f07b4db4307a2d06c5efcf64cc1
Source noteuspto-grants-2007_12