Réaction #56351

ord-ba1ca4c61eb1457a9d64e45728daff2e

Équation de réaction

C=CC(=O)OCCOC(=O)C=C
ethylene diacrylate
C=CC(=O)OCC
ethyl acrylate
C=C
ethylene
C=C
ethylene
C=CC(=O)OCCOC(=O)C=C
ethylene diacrylate
O=C1C=CC(=O)O1
maleic anhydride
C=CCOC(=O)C=C
allyl acrylate
→
C=C.C=CC(=O)OCC.C=CC(=O)OCCOC(=O)C=C.O=C1C=CC(=O)O1
Ethylene/Ethyl Acrylate Ethylene Diacrylate Maleic Anhydride

Réactifs

C=CC(=O)OCCOC(=O)C=C
ethylene diacrylate
C=CC(=O)OCC
ethyl acrylate
C=C
ethylene
C=C
ethylene
C=CC(=O)OCCOC(=O)C=C
ethylene diacrylate
O=C1C=CC(=O)O1
maleic anhydride
C=CCOC(=O)C=C
allyl acrylate

Réactifs

Aucun

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe branched tetrapolymer obtained

Mode opératoire

The procedure of D(1) above, was repeated except that 1.2 grams of ethylene diacrylate were used in place of the allyl acrylate. Yield: 479 grams. The branched tetrapolymer obtained had about 50 mole percent of ethylene units. The polymer chain consisted principally of units -(E)-(B')-, where E is ethylene and B' is randomly selected from ethyl acrylate, ethylene diacrylate, and maleic anhydride (3.8 weight percent).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04225476uspto-grants-1980_09