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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176207Generated: October 26, 2026

2-Phenylvinyl acetate → Hydroxystyrene amyloxystyrene

https://huagongshe.com/reaction/2176207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylvinyl acetateHCID 114576—
ReactantAmyloxystyreneHCID 54173547—
ProductHydroxystyrene amyloxystyreneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09063421B2
Source datasetuspto-grants-2015_06
ORD IDord-f3458857f2fe4d50a51a87cfe86df807
Source noteuspto-grants-2015_06