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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914434Generated: October 27, 2026

Methacrylic Acid → Methyl methacrylate methoxyethyl acrylate benzyl methacrylate methacrylic acid

https://huagongshe.com/reaction/1914434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantMethyl MethacrylateHCID 6658—
ReactantBenzyl methacrylateHCID 17236—
Reactant2-Methoxyethyl acrylateHCID 18392—
Reactant1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate)HCID 75763—
SolventMethyl Ethyl KetoneHCID 6569—
ProductMethyl methacrylate methoxyethyl acrylate benzyl methacrylate methacrylic acidHCID 131730237—

Reaction Conditions

Temperature75 °C

Reaction Steps

In a 2-L three-necked flask equipped with a stirrer, a thermometer, a reflux condenser, and a nitrogen gas introducing pipe, 360.0 g of methyl ethyl ketone was charged, and the temperature was increased to 75° C. A mixed solution containing 180 g of methyl methacrylate, 32.4 g of methoxyethyl acrylate, 126.0 g of benzyl methacrylate, 21.6 g of methacrylic acid, 72 g of methyl ethyl ketone, and 1.44 g of dimethyl-2,2-azobis(2-methylpropionate) (V-601, available from Wako Pure Chemical Industries, Ltd.) was added dropwise to the reactor at a constant speed for completing the dropwise addition in 2 hours. After the completion of the dropwise addition, a solution containing 0.72 g of “V-601” and 36.0 g of methyl ethyl ketone was added, and the resulting mixture was stirred at 75° C. for 2 hours. Thereafter, a solution containing 0.72 g of “V-601” and 36.0 g of methyl ethyl ketone was further added, and the resulting mixture was stirred at 75° C. for 2 hours. Thereafter, the temperature was increased to 85° C., and the mixture was continuously stirred for an additional 2 hours to obtain a resin solution of a methyl methacrylate/methoxyethyl acrylate/benzyl methacrylate/methacrylic acid (=50/9/35/6 [mass ratio]) copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08613510B2
Source datasetuspto-grants-2013_12
ORD IDord-441a6147f18d4039a7e5cff762ddb44b
Source noteuspto-grants-2013_12