HCID 54450032, compound → HCID 86757384, 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].[CH3:16][CH:17]([C:28]([OH:30])=[O:29])[CH2:18][CH2:19][CH2:20][CH2:21][CH:22]=[CH:23][CH2:24][CH2:25][CH2:26][CH3:27]>>[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].[CH3:16][CH:17]([C:28]([O-:30])=[O:29])[CH2:18][CH2:19][CH2:20][CH2:21][CH:22]=[CH:23][CH2:24][CH2:25][CH2:26][CH3:27].[C:13]1(=[O:15])[O:14][C:4](=[O:29])[CH:3]=[CH:2]1Participants
4
Procedure
The procedure according to Example 92 is repeated but using 2-methyl-11,12-dioxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylic acid (0.07 mole) as the third comonomer instead of 2-methyl-12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylic acid monomer (0.07 mole), to obtain poly(tert-butyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/2-methyl-11,12-dioxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylic acid/2-hydroxyethyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/maleic anhydride) represented by the following Chemical Formula 193:
Sources & evidence
- ORD record
- ord-ba3842041f504b2da36971b6222ecb92
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06291131B1
Reaction notes
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