HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473740Generated: October 26, 2026
2-Phenylvinyl acetate → Hydroxystyrene amyloxystyrene
https://huagongshe.com/reaction/1473740
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Phenylvinyl acetate | HCID 114576 | — |
| Reactant | Amyloxystyrene | HCID 54173547 | — |
| Product | Hydroxystyrene amyloxystyrene | HCID 86685023 | — |
Reaction Steps
The polymer used herein may be synthesized by any desired methods, for example, by dissolving acetoxystyrene and amyloxystyrene monomers in an organic solvent, adding a radical initiator thereto, effecting heat polymerization, and subjecting the resulting polymer to alkaline hydrolysis in the organic solvent to deprotect the acetoxy group, thereby obtaining a hydroxystyrene-amyloxystyrene copolymer. Examples of the organic solvent which can be used for polymerization include toluene, benzene, tetrahydrofuran, diethyl ether and dioxane. Examples of the polymerization initiator used herein include 2,2′-azobisisobutyronitrile (AIBN), 2,2′-azobis(2,4-dimethylvaleronitrile), dimethyl 2,2-azobis(2-methylpropionate), benzoyl peroxide, and lauroyl peroxide. Preferably the system is heated at 50 to 80° C. for polymerization to take place. The reaction time is 2 to 100 hours, preferably 5 to 20 hours. For the alkaline hydrolysis, aqueous ammonia, triethylamine or the like may be used as the base. The reaction temperature is −20° C. to 100° C., preferably 0° C. to 60° C., and the reaction time is 0.2 to 100 hours, preferably 0.5 to 20 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09017905B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-6df40590675844a296ac792ac11c408b |
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| Source note | uspto-grants-2015_04 |
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