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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191183Generated: October 25, 2026

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

https://huagongshe.com/reaction/2191183

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 numberUS08329380B2
Source datasetuspto-grants-2012_12
ORD IDord-eea102a0359147e8bd9c9a268912ecc2
Source noteuspto-grants-2012_12