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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425623Generated: October 25, 2026

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

https://huagongshe.com/reaction/1425623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidyl acrylateHCID 7836—
Reactant2-Hydroxyethyl MethacrylateHCID 13360—
Reactant1-Benzyloxyethyl methacrylateHCID 21834987—
Reactant2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
SolventMethyl Isobutyl KetoneHCID 7909—
SolventHeptaneHCID 8900—
Product1-Ethoxy-2-(2-methoxyethoxy)ethaneHCID 13847—
Product1-Benzyloxyethyl methacrylate glycidyl acrylate 2-hydroxyethyl methacrylateHCID 86643208—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08932800B2
Source datasetuspto-grants-2015_01
ORD IDord-b3787d17c7bc48b2a47dcf60f33a256d
Source noteuspto-grants-2015_01