Azobisisobutyronitrile → 2-Hydroxyethyl 5-norbornene-2-carboxylate t-butyl 5-norbornene-2-carboxylate 5-norbornene 2-carboxylic acid maleic anhydride

HRID 983760Notes

Reaction equation

HRID 983760 reaction equation
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH:8]12[CH2:14][CH:11]([CH:12]=[CH:13]1)[CH2:10][CH:9]2[C:15]([O:17][CH2:18][CH2:19][OH:20])=[O:16].[CH:21]12[CH2:27][CH:24]([CH:25]=[CH:26]1)[CH2:23][CH:22]2[C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29].[CH:35]12[CH2:41][CH:38]([CH:39]=[CH:40]1)[CH2:37][CH:36]2[C:42]([OH:44])=[O:43].N(C(C)(C)C#N)=NC(C)(C)C#N>O1CCCC1.C1(C)C=CC=CC=1>[CH:8]12[CH2:14][CH:11]([CH:12]=[CH:13]1)[CH2:10][CH:9]2[C:15]([O:17][CH2:18][CH2:19][OH:20])=[O:16].[CH:21]12[CH2:27][CH:24]([CH:25]=[CH:26]1)[CH2:23][CH:22]2[C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29].[CH:35]12[CH2:41][CH:38]([CH:39]=[CH:40]1)[CH2:37][CH:36]2[C:42]([OH:44])=[O:43].[C:4]1(=[O:5])[O:6][C:1](=[O:7])[CH:2]=[CH:3]1

Participants

8

Procedure

1 mole of maleic anhydride, 0.05-0.8 moles of 2-hydroxyethyl 5-norbornene-2-carboxylate, 0.5-0.95 moles of t-butyl 5-norbornene-2-carboxylate and 0.01 to 0.2 moles of 5-norbornene 2-carboxylic acid are dissolved in tetrahydrofuran or toluene. A radical reaction is executed at a temperature of about 60-70° C. for 4-24 hours under a nitrogen or argon atmosphere in the presence of 0.5-10 g of azobisisobutyronitrile (AIBN), as an initiator. The resin thus produced by this polymerization is precipitated in ethyl ether or hexane and dried to yield poly [2-hydroxyethyl 5-norbornene-2-carboxylate/t-butyl 5-norbornene-2-carboxylate/5-norbornene 2-carboxylic acid/maleic anhydride] resin of the following Formula X.

Workup

  1. customA radical reaction
  2. customThe resin thus produced by this polymerization
  3. customis precipitated in ethyl ether
  4. dry with materialhexane and dried

Sources & evidence

ORD record
ord-9ae56397a50040d58e2e67f9715b9d33
Source dataset
uspto-grants-2005_03
Patent number
US06866984B2

Reaction notes

Loading…