HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618844Generated: November 1, 2026
Glycidyl methacrylate → Propylene glycol methyl ether acetate
https://huagongshe.com/reaction/1618844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycidyl methacrylate | HCID 7837 | — |
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Reactant | 1-Butoxyethyl methacrylate | HCID 21959950 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Propylene glycol methyl ether acetate | HCID 7946 | — |
| Product | 1-n-Butoxyethyl methacrylate glycidyl methacrylate | HCID 86643206 | — |
Reaction Steps
A 500 ml three-necked flask was charged with 67.1 g (0.36 mol) of 1-n-butoxyethyl methacrylate, 34.1 g (0.24 mol) of glycidyl methacrylate and 300 ml of methyl isobutyl ketone. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) as a radical polymerization initiator was added to the mixture, and polymerization was performed in a nitrogen stream at 80° C. for six hours. The obtained reaction liquid was cooled, and poured in a large volume of heptane, thereby precipitating a polymer. The polymer crystal was collected by filtration, and dissolved in propylene glycol monomethyl ether acetate. The heptane and methyl isobutyl ketone contained in the solution were distilled off in vacuum, thereby obtaining a propylene glycol monomethyl ether acetate solution of polymer A-1 (1-n-butoxyethyl methacrylate/glycidyl methacrylate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08771907B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-732cc4fcff444f2f846c9ab40e5e0d26 |
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| Source note | uspto-grants-2014_07 |
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