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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1936531Erstellt: 25. Oktober 2026

Azobisisobutyronitrile → Di-tert-butyl 5-norbornene-2,3-dicarboxylate 2-hydroxyethyl 5-norbomene-2-carboxylate 5-norbomene-2,3-dicarboxylic acid maleic anhydride

https://huagongshe.com/reaction/1936531

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktMaleic AnhydrideHCID 7923—
Edukt5-Norbornene-2,3-dicarboxylic acidHCID 97965—
Edukt2-Hydroxyethyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 12033823—
Edukt5,6-Di(t-butoxycarbonyl)norborneneHCID 21922317—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDi-tert-butyl 5-norbornene-2,3-dicarboxylate 2-hydroxyethyl 5-norbomene-2-carboxylate 5-norbomene-2,3-dicarboxylic acid maleic anhydrideHCID 13172322031%

Reaktionsbedingungen

Temperatur67 °C

Reaktionsschritte

Di-tert-butyl 5-norbornene-2,3-dicarboxylate (0.85 mole), 2-hydroxyethyl 5-norbomene-2-carboxylate (0.1 mole), 5-norbornene-2,3-dicarboxylic acid (0.05 mole) and maleic anhydride (1 mole) were mixed together in tetrahydrofuran solvent, and AIBN (5.5 g) was added to the mixture as a polymerization initiator. Polymerization was performed under nitrogen atmosphere for 10 hours while maintaining the temperature at 67° C. When the polymerization was completed, the polymer was precipitated from ethyl ether and dried in vacuo to obtain pure poly(di-tert-butyl 5-norbornene-2,3-dicarboxylate/2-hydroxyethyl 5-norbomene-2-carboxylate/5-norbomene-2,3-dicarboxylic acid/maleic anhydride) of Chemical Formula 102 shown above (yield: 31%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06391518B1
Quelldatensatzuspto-grants-2002_05
ORD IDord-cfcd4e982b184ff0a6b8ca716104163c
Quellennotizuspto-grants-2002_05