Water → Dicyclopentadiene
Reaction equation
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]1[CH:12]2[CH:13]3[CH:17]=[CH:16][CH:15]([CH:11]2[CH:10]=[CH:9]1)[CH2:14]3.[OH2:18]>>[C:1]([OH:6])(=[O:7])/[CH:2]=[CH:3]\[C:4]([OH:18])=[O:5].[CH2:8]1[CH:12]2[CH:13]3[CH:17]=[CH:16][CH:15]([CH:11]2[CH:10]=[CH:9]1)[CH2:14]3Participants
Procedure
196 parts maleic anhydride, 278 parts (95% pure) dicyclopentadiene and 36 parts demineralized water were placed into a four-necked flask, and addition reaction was performed under nitrogen stream at 130° C. for 3 hours to obtain an addition product of maleic acid to dicyclopentadiene. Next, 392 parts maleic anhydride, 592 parts phthalic anhydride and 718 parts propylene glycol were added and mixed. Then the mixture was dehydrated and condensed in a widely-used manner under nitrogen stream at 200° C. for 8 hours to obtain a dicyclopentenyl-group-containing unsaturated polyester having an acid value of 25 mgKOH/g. This dicyclopentenyl-group-containing unsaturated polyester was dissolved at 80° C. in a solution in which 0.31 parts hydroquinone is dissolved in 1094 parts styrene monomer. A dicyclopentenyl-group-containing unsaturated polyester resin (III) of a viscosity of 4.5 stokes/25° C. was thus obtained.
Workup
- customwere placed into a four-necked flask
- additionaddition reaction
- customat 130° C.
- customfor 3 hours
Sources & evidence
- ORD record
- ord-6735c05070ce485f8c8294a405e98447
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05770653
Reaction notes
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