Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | 4-Vinylphenol | HCID 62453 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | 1-Methoxy-2-propanol | HCID 7900 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86655423 | HCID 86655423 | — |
Reaction Steps
p-t-butoxystyrene and ethyl vinyl ether (100 parts by mass in total (molar ratio: 60:40)) 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 into 4-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 random copolymer (4-hydroxystyrene/ethyl vinyl ether copolymer) (hereinafter referred to as “copolymer (AR-1)”). The copolymer (AR-1) was analyzed in the same manner as in Production Example 1. The copolymer (AR-1) had a content of the structural unit (ar1) derived from 4-hydroxystyrene of 60 mol %, and a content of the structural unit (ar2) derived from ethyl vinyl ether of 40 mol %. The copolymer (AR-1) had a polystyrene-reduced weight average molecular weight of 30,000, and a molecular weight distribution of 3.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247481B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-834b7aa651fe41a09ee71eb08706cba1 |
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| Source note | uspto-grants-2012_08 |
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