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HRID 1425626作成日:2026年10月27日

2-Hydroxyethyl Methacrylate → 1-Ethoxy-2-(2-methoxyethoxy)ethane

https://huagongshe.com/reaction/1425626

反応式

関与物質

役割名称HCID仕込み量
反応物2-Hydroxyethyl MethacrylateHCID 13360—
反応物2-((4-Ethenylphenoxy)methyl)oxiraneHCID 102865—
反応物Tetrahydropyranyl methacrylateHCID 11041138—
反応物2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
溶媒Methyl Isobutyl KetoneHCID 7909—
溶媒HeptaneHCID 8900—
生成物1-Ethoxy-2-(2-methoxyethoxy)ethaneHCID 13847—
生成物2-Tetrahydropyranyl methacrylate p-vinylphenyl glycidyl ether 2-hydroxyethyl methacrylateHCID 86643211—

反応手順

Into a 500 ml-volume three-neck flask, 57.0 g (0.36 mol) of 2-tetrahydropyranyl methacrylate, 31.7 g (0.18 mol) of p-vinylphenyl glycidyl ether, 7.8 g (0.06 mol) of 2-hydroxyethyl methacrylate and 300 ml of methyl isobutyl ketone were charged. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) was added thereto as a radical polymerization initiator, and polymerization was allowed to proceed at 80° C. for 6 hours in a nitrogen stream. The reaction solution was cooled and then poured in a large amount of heptane to precipitate a polymer. The crystal was collected by filtration and dissolved in diethylene glycol ethyl methyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-6 (2-tetrahydropyranyl methacrylate/p-vinylphenyl glycidyl ether/2-hydroxyethyl methacrylate) as a diethylene glycol ethyl methyl ether solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08932800B2
出典データセットuspto-grants-2015_01
ORD IDord-1cf600eea8b24d5da9ea525fb26e7e72
出典メモuspto-grants-2015_01