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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574029Generated: October 25, 2026

Glycidyl methacrylate → Glycidyl methacrylate 1-ethoxyethyl methacrylate 2-hydroxyethyl methacrylate

https://huagongshe.com/reaction/574029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidyl methacrylateHCID 7837—
Reactant2-Hydroxyethyl MethacrylateHCID 13360—
Reactant1-Ethoxyethyl Methacrylate (stabilized with MEHQ)HCID 20193345—
Reactant2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
SolventMethyl Isobutyl KetoneHCID 7909—
SolventHeptaneHCID 8900—
ProductGlycidyl methacrylate 1-ethoxyethyl methacrylate 2-hydroxyethyl methacrylateHCID 86655548—

Reaction Steps

Into a 500 ml-volume three-neck flask, 34.1 g (0.24 mol) of glycidyl methacrylate, 38.0 g (0.24 mol) of 1-ethoxyethyl methacrylate, 15.6 g (0.12 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 A2-5 (glycidyl methacrylate/1-ethoxyethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034440B2
Source datasetuspto-grants-2015_05
ORD IDord-204fa06f3d8e429185bac02a4d80c1cf
Source noteuspto-grants-2015_05