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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296596Generated: October 25, 2026

Maleic Anhydride → Furan-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-ene

https://huagongshe.com/reaction/2296596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
ReactantTetrahydrofuranHCID 8028—
CatalystAzobisisobutyronitrileHCID 6547—
SolventHexaneHCID 8058—
ProductFuran-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-eneHCID 287853183.7%

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 70 C. 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489082B1
Source datasetuspto-grants-2002_12
ORD IDord-1047302d657c4c47b2d228796d2cf922
Source noteuspto-grants-2002_12