HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369359Generated: October 26, 2026
Azobisisobutyronitrile → 2-Methyl-2-Adamantyl Methacrylate 2-Norbornene Maleic Anhydride
https://huagongshe.com/reaction/1369359
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 2-Norbornene | HCID 10352 | — |
| Reactant | 2-Methyl-2-adamantyl methacrylate | HCID 9837566 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-2-Adamantyl Methacrylate 2-Norbornene Maleic Anhydride | HCID 86583985 | 64.1% |
Reaction Steps
2-Methyl-2-adamantyl methacrylate, 2-norbornene and maleic anhydride were charged at a molar ratio of 4:3:3 (58.2 g:18.8 g:19.6 g). Thereto, tetrahydrofuran, the amount thereof being two times by weight based on the whole monomers, was added to form a monomer solution, followed by raising the temperature to 65° C. under nitrogen atmosphere. Then, was added azobisisobutyronitrile as an initiator in an amount of 3 mol % based on the whole monomer, and the resulting mixture was kept at 65° C. for 15 hours with stirring. Thereafter, the reaction mass was poured into a large amount of methanol to cause precipitation. This operation was repeated three times. A copolymer having a molecular weight of about 4710 and a molecular weight dispersion of 1.49 was obtained (61.9 g, yield 64.1%). This is called Resin AY.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579659B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-2ac923fa548247d2b87bbcb2db618b88 |
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| Source note | uspto-grants-2003_06 |
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