HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23858Generated: October 23, 2026
Maleic Anhydride → Furan-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-ene
https://huagongshe.com/en/reaction/23858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Furan-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-ene | HCID 287853 | 183.7% |
Reaction Steps
This synthesis example is directed to the synthesis of polymer (1b) (illustrated below as chemical formulas 14 or 15), a γ-hydroxy carboxylic acid structure. 21.2 g of 5-ethylenebicyclo[2.2.1]hept-2-ene, 19.6 g of maleic anhydride, 2.56 g of 2,2′-azobisisobutyronitrile, and 240 g of tetrahydrofuran were placed in a 500-ml, three-necked flask equipped with a thermometer, a condenser pipe, and a nitrogen inlet pipe, and the mixture was heated under reflux at 70C while introducing nitrogen for 8 hr to conduct polymerization. After the completion of the polymerization, the reaction mixture was poured into 1000 ml of n-hexane to precipitate the resultant polymer, which was then dried to give 37.5 g of a 5-methylenebicyclo[2.2.1]hept-2-ene/maleic anhydride copolymer (1a) (yield 92%). The polymer was analyzed by various methods and was found to mainly have a structure represented by the following formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06855483B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-798ec26d93734613be60fae168b8210e |
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| Source note | uspto-grants-2005_02 |
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