Maleic Anhydride → 8-ethyl-8-tricyclo[5.2.1.02,6]decanyl-5-norbornene-2-carboxylate maleic Anhydride cis-5-norbornene-endo-2,3-dicarboxylic Anhydride 2-hydroxyethyl-5-norbornene-2-carboxylate
Reaction equation
[CH2:1]([C:3]1([C:13]23[CH2:19][CH:16]([CH:17]=[CH:18]2)[CH2:15][CH:14]3[C:20]([O-:22])=[O:21])[CH2:11][CH:10]2[CH2:12][CH:4]1[CH:5]1[CH:9]2[CH2:8][CH2:7][CH2:6]1)[CH3:2].[C:23]1(=[O:29])[O:28][C:26](=[O:27])[CH:25]=[CH:24]1.[CH2:30]1[C@@H:34]2[CH:35]3[C:40](=[O:41])[O:39][C:37](=[O:38])[CH:36]3[C@H:31]1[CH:32]=[CH:33]2.[C:42]([O:46][CH2:47][CH2:48][OH:49])(=[O:45])[CH:43]=[CH2:44]>>[CH2:1]([C:3]1([C:13]23[CH2:19][CH:16]([CH:17]=[CH:18]2)[CH2:15][CH:14]3[C:20]([O-:22])=[O:21])[CH2:11][CH:10]2[CH2:12][CH:4]1[CH:5]1[CH:9]2[CH2:8][CH2:7][CH2:6]1)[CH3:2].[C:26]1(=[O:27])[O:28][C:23](=[O:29])[CH:24]=[CH:25]1.[CH2:30]1[C@@H:34]2[CH:35]3[C:40](=[O:41])[O:39][C:37](=[O:38])[CH:36]3[C@H:31]1[CH:32]=[CH:33]2.[OH:49][CH2:48][CH2:47][O:46][C:42]([CH:43]1[CH2:4][CH:3]2[CH2:11][CH:44]1[CH:2]=[CH:1]2)=[O:45]Participants
5
Reactant 4
Product 1
Procedure
Polymerization and separation were carried out in the same manner as in Example 18 using 75 mmol of 8-ethyl-8-tricyclo[5.2.1.02,6]decanyl-5-norbornene-2-carboxylate prepared in Example 3, 100 mmol of maleic anhydride, 15 mmol of cis-5-norbornene-endo-2,3-dicarboxylic anhydride and 10 mmol of 2-hydroxyethyl acrylate, to separate 5.74 g of a polymer.
Workup
- customPolymerization and separation
- customto separate 5.74 g of a polymer
Sources & evidence
- ORD record
- ord-a51810f6f351402b8ee91b89463ab9b3
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06642336B1
Reaction notes
Loading…