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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516279Generated: October 30, 2026

tert-Butyl hydroperoxide → Glycidyl methacrylate

https://huagongshe.com/reaction/516279

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantMethyl MethacrylateHCID 6658—
ReactantStyreneHCID 7501—
ReactantButyl AcrylateHCID 8846—
SolventWaterHCID 962—
ProductGlycidyl methacrylateHCID 7837—

Reaction Conditions

Temperature70 °C

Reaction Steps

An amount of 1300 g of an aqueous latex of a core polymer mainly comprising a styrene-butadiene rubber (containing 420 g of styrene-butadiene rubber particles) as obtained using the procedure described in Example 2 was charged into a 3 L glass vessel followed by addition of 440 g of pure water and stirring at 70° C. while replacing the atmosphere inside the vessel with nitrogen. A monomer mixture composed of 60 g of methyl methacrylate, 10 g of butyl acrylate, 35 g of styrene and 0.4 g of t-butyl hydroperoxide as a monomer mixture that is not the shell forming monomers (A) was added thereto over the course of 120 minutes to carry out graft polymerization. Following completion of the addition of the monomer mixture, stirring was further continued for 2 hours to complete the reaction and obtain minute polymer particles (CS-2C) in the form of an aqueous latex. The polymerization conversion rate was 99%. As a result of measuring the particle size in the same manner as in Example 2 after diluting the minute polymer particles in the form of an aqueous latex with water, the measured particle size was 0.1 μm, and a sharp, monodisperse particle size distribution nearly similar to that of Example 2 was shown.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09109069B2
Source datasetuspto-grants-2015_08
ORD IDord-9154d8d908554dea92cb0f1896fc03e1
Source noteuspto-grants-2015_08