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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycidyl acrylate | HCID 7836 | — |
| Reactant | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Reactant | 1-Benzyloxyethyl methacrylate | HCID 21834987 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| Product | 1-Benzyloxyethyl methacrylate glycidyl acrylate 2-hydroxyethyl methacrylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08329380B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-eea102a0359147e8bd9c9a268912ecc2 |
|---|
| Source note | uspto-grants-2012_12 |
|---|