Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1-Methoxy-2-propanol | HCID 7900 | — |
| Reactant | Hydroxystyrene | HCID 138202 | — |
| Reactant | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19083679 | HCID 19083679 | — |
Reaction Steps
A solution was prepared by dissolving 100 parts by weight, as the total amount, of p-t-butoxystyrene and styrene (molar ratio was p-t-butoxystyrene:styrene=80:20) in 150 parts by weight of propylene glycol monomethyl ether. This solution was kept under a nitrogen atmosphere at 70° C. for 10 hr with 4 parts by weight of azobisisobutyronitrile supplied to proceed polymerization. Then, sulfuric acid was added to the reaction solution, and the resultant solution was kept at 90° C. for 10 hr to covert the p-t-butoxystyrene unit into a hydroxystyrene unit through deprotection. Ethyl acetate was added to the obtained copolymer, the resultant solution was washed with water 5 times, the ethyl acetate phase was collected, and the solvent was removed to obtain p-hydroxystyrene/styrene copolymer (hereinafter, referred as “alkali soluble resin (A-1)”).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07332254B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-b0b0b76442ad4b05b3d8cde5fcbb7f29 |
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| Source note | uspto-grants-2008_02 |
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