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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1425625Erstellt: 26. Oktober 2026

2-Hydroxyethyl Methacrylate → 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate

https://huagongshe.com/reaction/1425625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Hydroxyethyl MethacrylateHCID 13360—
Edukt(7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoateHCID 14645478—
Edukt2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
Edukt1-Cyclohexyloxyethyl methacrylateHCID 22995281—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
LösungsmittelHeptaneHCID 8900—
Produkt1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylateHCID 86643210—

Reaktionsschritte

Into a 500 ml-volume three-neck flask, 76.4 g (0.36 mol) of 1-cyclohexyloxyethyl methacrylate, 35.3 g (0.18 mol) of 3,4-epoxycyclohexylmethyl methacrylate (Cyclomer M100, produced by Daicel Chemical Industries, Ltd.), 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 dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-5 (1-cyclohexyloxyethyl methacrylate/3,4-epoxycyclohexylmethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08932800B2
Quelldatensatzuspto-grants-2015_01
ORD IDord-4698e2394c2b4f6990241ab9f73e7f12
Quellennotizuspto-grants-2015_01