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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482661Generated: November 1, 2026

Glycidyl methacrylate → 2-Hydroxyethyl Methacrylate

https://huagongshe.com/reaction/482661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidyl methacrylateHCID 7837—
ReactantHCID 88748020HCID 88748020—
Product2-Hydroxyethyl MethacrylateHCID 13360—
ProductHCID 131714533HCID 131714533—

Reaction Steps

The terpolymer (butadiene-styrene-HEMA) of Example 1 was compounded as in Example 1. A butadiene-styrene-glycidyl methacrylate (GMA) terpolymer was prepared using Recipe C (Table I), it was stripped, coagulated and compounded as in Example 1. The oil extended GMA terpolymer had a Mooney of 91. As seen from Table 3, the HEMA terpolymer gave compounds having better vibrotester resilience than compounds of the GMA terpolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04574140
Source datasetuspto-grants-1986_03
ORD IDord-10270e7645ff49ff90d2128b96f0dedb
Source noteuspto-grants-1986_03