Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574020Generated: October 26, 2026

2-Hydroxyethyl Methacrylate → 1-Ethoxy-2-(2-methoxyethoxy)ethane

https://huagongshe.com/reaction/574020

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxyethyl MethacrylateHCID 13360—
ReactantBenzyl methacrylateHCID 17236—
Reactant1-Ethoxyethyl Methacrylate (stabilized with MEHQ)HCID 20193345—
Reactant2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
SolventMethyl Isobutyl KetoneHCID 7909—
SolventHeptaneHCID 8900—
Product1-Ethoxy-2-(2-methoxyethoxy)ethaneHCID 13847—
Product1-Ethoxyethyl methacrylate benzyl methacrylate 2-hydroxyethyl methacrylateHCID 67322267—

Reaction Steps

Into a 500 ml-volume three-neck flask, 66.4 g (0.42 mol) of 1-ethoxyethyl methacrylate, 21.1 g (0.12 mol) of benzyl methacrylate, 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 A1-3 (1-ethoxyethyl methacrylate/benzyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol ethyl methyl ether solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034440B2
Source datasetuspto-grants-2015_05
ORD IDord-a8173f061ccd4c208b44f6df00abba57
Source noteuspto-grants-2015_05