Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | 1-Methoxy-2-propanol | HCID 7900 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86643781 | HCID 86643781 | — |
Reaction Steps
1 part by mass of divinylbenzene (manufactured by Nippon Steel Chemical Co., Ltd., purity: 57 mass %), 60 parts by mass of p-t-butoxystyrene, and 4 parts by mass of styrene were dissolved in 150 parts by mass of propylene glycol monomethyl ether. The mixture was polymerized at 70° C. for 10 hours in a nitrogen atmosphere in the presence of 4 parts by mass of azobisisobutyronitrile. After the addition of sulfuric acid to the reaction solution, the components were reacted at 90° C. for 10 hours to convert (deprotect) p-t-butoxystyrene to p-hydroxystyrene. After the addition of ethyl acetate to the resulting copolymer, the mixture was washed five times with water. After isolating the ethyl acetate phase, the solvent was removed to obtain a divinylbenzene/p-hydroxystyrene/styrene copolymer (hereinafter referred to as “resin (A-1)”). The resin (A-1) was analyzed by 13C-NMR. The resin (A-1) had a content of the structural unit (a1-1) derived from divinylbenzene of 1 mol %, a content of the structural unit (a2) derived from p-hydroxystyrene of 89 mol %, and a content of the structural unit (a3-1) derived from styrene of 10 mol %. The resin (A-1) had a polystyrene-reduced weight average molecular weight of 24,000.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455173B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-b2037b941c0f44b69c46d933a1f8181f |
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| Source note | uspto-grants-2013_06 |
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