Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | Glycidyl acrylate | HCID 7836 | — |
| Reactant | Glycidyl methacrylate | HCID 7837 | — |
| Reactant | Allyl glycidyl ether | HCID 7838 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | ((o-Allylphenoxy)methyl)oxirane | HCID 98437 | — |
| Reactant | Methallyl glycidyl ether | HCID 13668594 | — |
| Reactant | Crotyl phenyl glycidyl ether | HCID 131710954 | — |
| Product | Bisphenol A | HCID 6623 | — |
| Product | Epichlorohydrin | HCID 7835 | — |
Reaction Steps
Examples of the compound having an effectively photopolymerizable carbon-to-carbon double bond and a 1,2-epoxy group in the molecule and having a boiling point of at least 120° C. [component (B) (i)] are glycidyl acrylate, glycidyl methacrylate, glycidyl allyl ether, o-allyl phenyl glycidyl ether, crotyl phenyl glycidyl ether, methallyl glycidyl ether, epoxy acrylate type resins obtained by condensing a part of the epoxy group of the polyepoxy compound exemplified above as component (A) with acrylic acid or methacrylic acid, epoxy acrylate type resins obtained by adding acryloyl chloride to the side chain of the polyepoxy compound exemplified above as component (A), especially an epoxy resin obtained by the condensation of bisphenol A and epichlorohydrin, and polyepoxy compounds obtained by epoxidizing some of the many carbon-to-carbon double bonds present in polybutadiene obtained by anionic polymerization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04060656 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-08435dfe3bbf460099b988bf5a9276c2 |
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| Source note | uspto-grants-1977_11 |
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