HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycidyl methacrylate → 2-Hydroxyethyl Methacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycidyl methacrylate | HCID 7837 | — |
| Reactant | HCID 88748020 | HCID 88748020 | — |
| Product | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Product | HCID 131714533 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04574140 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-10270e7645ff49ff90d2128b96f0dedb |
| Source note | uspto-grants-1986_03 |