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HRID 1926557作成日:2026年10月27日

Azobisisobutyronitrile → Hydroxystyrene

https://huagongshe.com/reaction/1926557

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物tert-Butyl acrylateHCID 15458—
反応物4-Ethenylphenyl acetateHCID 75821—
反応物3-Hydroxy-1-methacryloyloxyadamantaneHCID 11856523—
溶媒TetrahydrofuranHCID 8028—
生成物HydroxystyreneHCID 138202—

反応手順

To a round bottom flask equipped with condenser, thermometer, an argon (Ar) inlet, and a magnetic stirrer bar, the following were added: 4-acetoxystyrene monomer (2.43 grams (g), 0.015 mole), t-butyl acrylate monomer (1.6 g, 0.0125 mole), 3-hydroxy-1-adamantyl methacrylate monomer (5.319 g, 0.0225 mole), 2,2′-azobis(2-methylpropionitrile) (AIBN)(0.328 g, 4% of total moles of monomers), and approximately 40 g of tetrahydrofuran (THF). The reaction mixture was stirred at room temperature and bubbled with Ar flow for 45 minutes before it was heated. The reaction was carried out overnight at 72° C. under an inert Ar atmosphere. The rest of the synthetic procedures are the same as Example 1, except approximately 5 g of concentrated NH4OH was used in deprotecting the acetoxy groups from acetoxystyrene repeat units to form hydroxyl styrene repeat units of the terpolymer.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08182978B2
出典データセットuspto-grants-2012_05
ORD IDord-5c2b9561a3cc46488d806c83fa21991d
出典メモuspto-grants-2012_05