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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232662Generated: October 27, 2026

2-Hydroxyethyl acrylate → Urethane acrylate

https://huagongshe.com/reaction/2232662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Hydroxyethyl acrylateHCID 13165—
Reactant4-[1,1,1,3,3,3-Hexafluoro-2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-olHCID 2782224—
ReactantIsophorone DI-isocyanateHCID 21298402—
Catalyst4-MethoxyphenolHCID 9015—
CatalystDi-n-butyldilauryltinHCID 9809426—
SolventAcetoneHCID 180—
ProductUrethane acrylateHCID 21863578821.4%

Reaction Steps

In 300 g of acetone were dissolved 46.2 g of isophoronediisocyanate, 70.3 g of 4,4'-(perfluoroisopropylidene)dicyclohexanol and 0.8 g of di-n-butyltin dilaurate. The mixture was reacted at 54° to 56° C. for 15 hours with stirring while introducing dry nitrogen. To the mixture were added 10 g of 2-hydroxyethyl acrylate, 0.4 g of di-n-butyltin dilaurate and 0.1 g of hydroquinone monomethyl ether and the mixture was reacted at 54° to 56° C. for 16 hours. A few drops of the reaction mixture were placed on KBr plate. The plate was dried and subjected to infrared absorption spectrum analysis to find an absorption based on isocyanate group (2250 cm-1) disappeared. The reaction mixture was poured into a large excess amount of hexane and the resulting precipitates were filtered, dried and pulverized to obtain 114 g of urethane acrylate in the form of white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788327
Source datasetuspto-grants-1988_11
ORD IDord-e0176e71a351451480f0d2f604d40f58
Source noteuspto-grants-1988_11