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HRID 496978作成日:2026年10月26日

2-Phenylvinyl acetate → Hydroxystyrene

https://huagongshe.com/reaction/496978

反応式

関与物質

役割名称HCID仕込み量
反応物2-Phenylvinyl acetateHCID 114576—
反応物AmyloxystyreneHCID 54173547—
生成物HydroxystyreneHCID 138202—
生成物AmyloxystyreneHCID 54173547—

反応手順

In one typical embodiment, the polymer can be synthesized by dissolving an acetoxystyrene monomer, a (meth)acrylic acid tertiary ester monomer and an amyloxystyrene monomer in an organic solvent, adding a radical initiator thereto, heat polymerizing the monomers, and subjecting the resulting polymer to alkaline hydrolysis in an organic solvent for deblocking the acetoxy group, thereby forming a ternary copolymer of hydroxystyrene, (meth)acrylic acid tertiary ester and amyloxystyrene. Examples of the organic solvent used in polymerization include toluene, benzene, tetrahydrofuran, diethyl ether, and dioxane. Representative of the polymerization initiator are 2,2′-azobisisobutyronitrile, 2,2′-azobis(2,4-dimethyl-valeronitrile), dimethyl-2,2-azobis(2-methylpropionate), benzoyl peroxide and lauroyl peroxide. Polymerization may be effected by heating at about 50 to 80° C. The reaction time is usually about 2 to 100 hours, preferably about 5 to 20 hours. The base used in the alkaline hydrolysis is selected from aqueous ammonia and triethylamine, to name a few. The reaction temperature is about −20° C. to 100° C., preferably about 0 to 60° C. The reaction time is usually about 0.2 to 100 hours, preferably about 0.5 to 20 hours.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06949323B2
出典データセットuspto-grants-2005_09
ORD IDord-7c9e780ecfc842609fca553328ebefb1
出典メモuspto-grants-2005_09