Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 840496Erstellt: 25. Oktober 2026

Azobisisobutyronitrile → Maleic anhydride mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo[2.2.1]hept-5-ene-2.3-dicarboxylate tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate 3-[tris(trimethylsiloxy)silyl]propyl methacrylate

https://huagongshe.com/reaction/840496

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzobisisobutyronitrileHCID 6547—
EduktMaleic AnhydrideHCID 7923—
Edukt3-(Tris(trimethylsiloxy)silyl)propyl methacrylateHCID 123371—
EduktBicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl esterHCID 15607334—
EduktMono-2-ethyl-2-(hydroxymethyl)butyl bicyclo-[2.2.1]hept-5-ene-2,3-dicarboxylateHCID 86757924—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMaleic anhydride mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo[2.2.1]hept-5-ene-2.3-dicarboxylate tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate 3-[tris(trimethylsiloxy)silyl]propyl methacrylateHCID 86757923—

Reaktionsschritte

1.0 mole of maleic anhydride, 0.2 mole of mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo-[2.2.1]hept-5-ene-2,3-dicarboxylate, 0.7 mole of tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate and 0.1 mole of 3-[tris(trimethylsiloxy)silyl]propyl methacrylate are dissolved in tetrahydrofuran, 0.5 to 10 g of AIBN is added thereto as the polymerization initiator, and the resultant mixture is reacted at approximately 60 to 70° C. for 4 to 24 hours under a nitrogen or argon atmosphere.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06368771B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-f453fa0f25164914b5f276ce420bb989
Quellennotizuspto-grants-2002_04