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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392980Generated: October 30, 2026

Ethylene Oxide → Urethane acrylate

https://huagongshe.com/reaction/2392980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
Reactant1,2-EpoxybutaneHCID 7834—
ReactantToluene 2,4-DiisocyanateHCID 11443—
Reactant2-Hydroxyethyl acrylateHCID 13165—
Reactant(3-Mercaptopropyl)trimethoxysilaneHCID 20473—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantIsocyanateHCID 105034—
ProductUrethane acrylateHCID 21863578—

Reaction Steps

Into a reaction vessel equipped with a stirrer were charged 3.0 parts of tolylene diisocyanate, 50.5 parts of a ring-opening copolymer from ethylene oxide and butene oxide, having a number average molecular weight of 4,000, and 0.01 part of 2,6-di-t-butyl-p-cresol, as a polymerization inhibitor. The mixture was cooled with ice to a temperature of below 10° C., while stirring. When the temperature was lower than 10° C., 0.04 part of dibutyltindilaurate was added and the mixture was stirred for 2 hours while controlling the temperature at 20°-30° C. Then, after the addition of 0.3 part of γ-mercaptopropyltrimethoxy silane, the mixture was stirred for a further one hour at 30°-40° C., whereupon 1.2 parts of hydroxyethyl acrylate was added. The mixture was stirred for 4 hours at 50°-60° C., until the amount of remaining isocyanate is 0.1% by weight or less. The liquid urethane acrylate obtained in this manner is hereinafter referred to as UA-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804311
Source datasetuspto-grants-1998_09
ORD IDord-ff00b5fe7579458aaf20cc6789b44d39
Source noteuspto-grants-1998_09