HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Katalysator | Azobisisobutyronitrile | HCID 6547 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | Furan-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-ene | HCID 287853 | 183,7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06017680 |
|---|
| Quelldatensatz | uspto-grants-2000_01 |
|---|
| ORD ID | ord-cfafbbf2288348c4bd66becc791ce7d5 |
|---|
| Quellennotiz | uspto-grants-2000_01 |
|---|