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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1425623생성일: 2026년 10월 27일

Glycidyl acrylate → 1-Ethoxy-2-(2-methoxyethoxy)ethane

https://huagongshe.com/reaction/1425623

반응식

참여 물질

역할이름HCID투입량
반응물Glycidyl acrylateHCID 7836—
반응물2-Hydroxyethyl MethacrylateHCID 13360—
반응물1-Benzyloxyethyl methacrylateHCID 21834987—
반응물2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
용매Methyl Isobutyl KetoneHCID 7909—
용매HeptaneHCID 8900—
생성물1-Ethoxy-2-(2-methoxyethoxy)ethaneHCID 13847—
생성물1-Benzyloxyethyl methacrylate glycidyl acrylate 2-hydroxyethyl methacrylateHCID 86643208—

반응 단계

Into a 500 ml-volume three-neck flask, 79.3 g (0.36 mol) of 1-benzyloxyethyl methacrylate, 23.1 g (0.18 mol) of glycidyl acrylate, 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-3 (1-benzyloxyethyl methacrylate/glycidyl acrylate/2-hydroxyethyl methacrylate) as a diethylene glycol ethyl methyl ether solution.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08932800B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-b3787d17c7bc48b2a47dcf60f33a256d
출처 메모uspto-grants-2015_01