HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618836Generated: October 26, 2026
Methyl Isobutyl Ketone → 1-Ethoxy-2-(2-methoxyethoxy)ethane
https://huagongshe.com/reaction/1618836
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | 4-Methoxystyrene | HCID 12507 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Reactant | 1-Cyclohexyloxyethyl methacrylate | HCID 22995281 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| Product | 1-Cyclohexyloxyethyl methacrylate p-methoxystyrene | HCID 86655543 | — |
Reaction Steps
A 500 ml three-necked flask was charged with 63.7 g (0.30 mol) of 1-cyclohexyloxyethyl methacrylate, 40.3 g (0.30 mol) of p-methoxystyrene 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 diethylene glycol ethyl methyl ether. The heptane and methyl isobutyl ketone contained in the solution were distilled off in vacuum, thereby obtaining a diethylene glycol ethyl methyl ether solution of polymer A1-6 (1-cyclohexyloxyethyl methacrylate/p-methoxystyrene).
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-0c1dc38fc8a143e0a6949641ff9a707d |
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| Source note | uspto-grants-2014_07 |
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