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HRID 850249Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/850249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMaleic AnhydrideHCID 7923—
EduktTetrahydrofuranHCID 8028—
KatalysatorAzobisisobutyronitrileHCID 6547—
LösungsmittelHexaneHCID 8058—
ProduktFuran-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-eneHCID 287853183,7%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06017680
Quelldatensatzuspto-grants-2000_01
ORD IDord-cfafbbf2288348c4bd66becc791ce7d5
Quellennotizuspto-grants-2000_01