HCID 54450032, compound → HCID 86757384, compound
Reaction equation
[CH3:1][CH:2]([C:16]([OH:18])=[O:17])[CH:3]([C:13]([OH:15])=O)[CH2:4][CH2:5][CH2:6][CH:7]=[CH:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:19][CH:20]([C:31]([OH:33])=[O:32])[CH2:21][CH2:22][CH2:23][CH2:24][CH:25]=[CH:26][CH2:27][CH2:28][CH2:29][CH3:30]>>[CH3:1][CH:2]([C:16]([O-:18])=[O:17])[CH2:3][CH2:4][CH2:5][CH2:6][CH:7]=[CH:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:19][CH:20]([C:31]([O-:33])=[O:32])[CH2:21][CH2:22][CH2:23][CH2:24][CH:25]=[CH:26][CH2:27][CH2:28][CH2:29][CH3:30].[C:16]1(=[O:17])[O:18][C:13](=[O:15])[CH:3]=[CH:2]1Participants
4
Procedure
The procedure according to Example 81 is repeated but using 11,12-dioxatetracyclo[4.4.0.1.1]dodec-7-ene-2,3-dicarboxylic acid (0.05 mole) as the third comonomer instead of 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylic acid (0.05 mole), to obtain poly(1,1-dimethylethyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/11,12-dioxatetracyclo[4.4.0.1.1]dodec-7-ene-2,3-dicarboxylic acid/2-hydroxyethyl 11,12-dioxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/maleic anhydride) represented by the following Chemical Formula 185:
Sources & evidence
- ORD record
- ord-d8bf637067fe4972ab03ac3af1ec55fa
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06291131B1
Reaction notes
Loading…