HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574023Generated: October 25, 2026
Methyl Isobutyl Ketone → 1-Ethoxy-2-(2-methoxyethoxy)ethane
https://huagongshe.com/reaction/574023
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
Into a 500 ml-volume three-neck flask, 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 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 A1-6 (1-cyclohexyloxyethyl methacrylate/p-methoxystyrene) as a diethylene glycol ethyl methyl ether solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034440B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-df2f0c3a92004fd3b7a54c24b2283ce0 |
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| Source note | uspto-grants-2015_05 |
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