HCID 86757387, compound → HCID 12914729, compound
Reaction equation
C[CH:2]([C:21]([OH:23])=[O:22])[CH:3]([C:18]([OH:20])=[O:19])[CH2:4][CH2:5][CH2:6]CCC=CCCCCCCC.[CH3:24][CH:25]([C:41]([OH:43])=[O:42])[CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH:32]=[CH:33][CH2:34][CH2:35]CCCCC>>[CH:4]12[O:23][CH:21]([CH:6]=[CH:5]1)[CH2:2][CH:3]2[C:18]([O:20][C:25]([CH3:41])([CH3:26])[CH3:24])=[O:19].[CH3:24][CH:25]([C:41]([O-:43])=[O:42])[CH2:26][CH2:27][CH2:28][CH2:29][CH:30]=[CH:31][CH2:32][CH2:33][CH2:34][CH3:35].[C:21]1(=[O:22])[O:23][C:18](=[O:20])[CH:3]=[CH:2]1Participants
4
Procedure
The procedure according to Example 86 is repeated but using 16,17-dioxahexacyclo[6.6.1.1.1.0.0]heptadec-9-ene-2,3-dicarboxylic acid monomer (0.07 mole) as the third comonomer instead of 15,16,17-trioxahexacyclo[6.6.1.1.1.0.0]heptadec-9-ene-2-carboxylic acid (0.07 mole), to obtain poly(1,1-dimethylethyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylate/16,17-dioxahexacyclo[6.6.1.1.1.0.0]heptadec-9-ene-2,3-dicarboxylic acid/2-hydroxyethyl 12-oxatetracyclo[4.4.0.1.1]dodec-7-ene-2-carboxylate/maleic anhydride) represented by the following Chemical Formula 188:
Sources & evidence
- ORD record
- ord-92c1177d2c6a463083938e4dec32b7f4
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06291131B1
Reaction notes
Loading…