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HRID 2191185作成日:2026年10月25日

2-Hydroxyethyl Methacrylate → 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate

https://huagongshe.com/reaction/2191185

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(7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoateHCID 14645478—
反応物2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
反応物1-Cyclohexyloxyethyl methacrylateHCID 22995281—
溶媒Methyl Isobutyl KetoneHCID 7909—
溶媒HeptaneHCID 8900—
生成物1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylateHCID 86643210—

反応手順

Into a 500 ml-volume three-neck flask, 76.4 g (0.36 mol) of 1-cyclohexyloxyethyl methacrylate, 35.3 g (0.18 mol) of 3,4-epoxycyclohexylmethyl methacrylate (Cyclomer M100, produced by Daicel Chemical Industries, Ltd.), 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 dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-5 (1-cyclohexyloxyethyl methacrylate/3,4-epoxycyclohexylmethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08329380B2
出典データセットuspto-grants-2012_12
ORD IDord-effc43291b5a4d58bf5cfcb7ee348b26
出典メモuspto-grants-2012_12