HCID 54450032, compound → HCID 86757385, compound
Reaction equation
[CH3:1][CH:2]([C:13]([O-:15])=[O:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[CH:8][CH2:9][CH2:10][CH2:11][CH3:12].C[CH:17]([C:28]([OH:30])=[O:29])[CH2:18][CH2:19]CCC=CCCCC>>[CH3:1][CH:2]([C:13]([O-:15])=[O:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[CH:8][CH2:9][CH2:10][CH2:11][CH3:12].[C:28]1(=[O:30])[O:29][C:19](=[O:14])[CH:18]=[CH:17]1Participants
3
Procedure
The procedure according to Example 76 is repeated but using 3-hydroxypropyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate as the second comonomer instead of 2-hydroxyethyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate (0.15 mole), and methyl 12-oxatetracyclo[4.4.0.1.1]dodecne-2,3-dicarboxylic acid (0.15 mole) as the third comonomer instead of 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylic acid monomer, to obtain poly(1,1-dimethylethyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/methyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2,3-dicarboxylic acid/3-hydroxypropyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/maleic anhydride) represented by the following Chemical Formula 196:
Sources & evidence
- ORD record
- ord-d3e9cc391fbe45929f8d72c93d9f3d3e
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06291131B1
Reaction notes
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