HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179098Generated: October 31, 2026
Azobisisobutyronitrile → HCID 131726626, compound
https://huagongshe.com/reaction/1179098
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | tert-Butyl methacrylate | HCID 11448 | — |
| Reactant | 3-(Trimethoxysilyl)propyl methacrylate | HCID 17318 | — |
| Reactant | Methyl bicyclo[2.2.1]hept-5-ene-2-carboxylate | HCID 250075 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131726626 | HCID 131726626 | — |
Reaction Steps
To 25 ml of tetrahydrofuran in 100 ml of a round-shaped flask were added 5 g of 3-(trimethoxysilyl)propyl methacrylate, 4 g of t-butyl methacrylate, 3 g of methyl 5-norbornene-2-carboxylate and 3 g of maleic anhydride. Then, 0.13 g of AIBN (azobisisobutyronitrile) as a polymerization initiator was added to the resulting mixture, and reacted at 67° C. under a nitrogen atmosphere for 24 hours. Next, the resulting mixture was cooled at room temperature, and poured into a beaker including 500 ml of ethyl ether to precipitate the resulting mixture. Thereafter, the precipitate was filtered and dehydrated at room temperature, thereby obtaining poly(3-(trimethyoxysilyl)propyl methacrylate/t-butyl methacrylate/methyl 5-norbornene-2-carboxylate/maleic anhydride) having a molecular weight of 1,800 represented by formula 1a (yield: 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279256B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-7a45437b565f4d20b1f5ced06ecb9bf2 |
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| Source note | uspto-grants-2007_10 |
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