Maleic Anhydride → HCID 86584310, compound
Reaction equation
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].[CH:15]12[CH2:21][CH:18]([CH:19]=[CH:20]1)[CH2:17][CH:16]2[CH2:22][CH:23]1[O:28][C:26](=[O:27])[CH2:25][CH2:24]1.[C:29]1(=[O:35])[O:34][C:32](=[O:33])[CH:31]=[CH:30]1>>[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2[C:8]([O:10][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:9].[CH:15]12[CH2:21][CH:18]([CH:19]=[CH:20]1)[CH2:17][CH:16]2[CH2:22][CH:23]1[O:28][C:26](=[O:27])[CH2:25][CH2:24]1.[C:32]1(=[O:33])[O:34][C:29](=[O:35])[CH:30]=[CH:31]1Participants
4
Procedure
Polymerization reaction of tert-butyl 5-norbornene-2-carboxylate, Monomer 1, and maleic anhydride was effected using an initiator V65 (Wako Junyaku K.K.), yielding an alternating copolymer of tert-butyl 5-norbornene-2-carboxylate/γ-(5-norbornen-2-yl)methyl-γ-butyrolactone/maleic anhydride (copolymerization ratio 4/1/5).
Sources & evidence
- ORD record
- ord-18b5dabc9d234fec8f07211ec2bdf499
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472543B2
Reaction notes
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