Reaction equation
[C:1]([O:5][CH2:6][CH2:7][O:8][C:9](=[O:12])[CH:10]=[CH2:11])(=[O:4])[CH:2]=[CH2:3].[C:13]1(=[O:19])[O:18][C:16](=[O:17])[CH:15]=[CH:14]1>>[CH2:1]=[CH2:2].[C:1]([O:5][CH2:6][CH3:7])(=[O:4])[CH:2]=[CH2:3].[C:1]([O:5][CH2:6][CH2:7][O:8][C:9](=[O:12])[CH:10]=[CH2:11])(=[O:4])[CH:2]=[CH2:3].[C:16]1(=[O:17])[O:18][C:13](=[O:19])[CH:14]=[CH:15]1Participants
3
Procedure
The procedure of Part D(1) was repeated except that 0.75 gram of ethylene diacrylate was used in place of allyl acrylate. Yield: 476 grams. 2.3 weight percent of maleic anhydride was present.
Sources & evidence
- ORD record
- ord-0590706f4cbb4586a2d75e14484f78e4
- Source dataset
- uspto-grants-1980_09
- Patent number
- US04225476
Linked notes
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