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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417012Generated: October 25, 2026

Trimethylolpropane → Urethane acrylate

https://huagongshe.com/reaction/2417012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropaneHCID 6510—
ReactantStearyl AlcoholHCID 8221—
Reactant4-MethoxyphenolHCID 9015—
Reactant1,3-Bis(isocyanatomethyl)benzeneHCID 19262—
ReactantBis(isocyanatomethyl)benzeneHCID 3035160—
ReactantDi-n-butyldilauryltinHCID 9809426—
SolventTolueneHCID 1140—
ProductUrethane acrylateHCID 21863578—

Reaction Conditions

Temperature40 °C

Reaction Steps

Into a flask similar to the flask in Synthesis Example 1 were charged 44.8 parts of toluene and 4.6 parts of stearyl alcohol (NAA-46), followed by heating of the mixture to 40° C. After the confirmation of thorough dissolution of stearyl alcohol, 50 parts of xylylene diisocyanate subjected to trimethylol-propane adduct modification (“TAKENATE D-110N” a trade name of Takeda Chemical Industries, Ltd., N.V.: 75, NCO %: 11.5) were charged and the mixture was heated to 70° C. After 30 minutes of the reaction at the same temperature, 0.02 parts of dibutyltin laurate were charged. After the mixture was maintained at the same temperature for 3 hours, 91.7 parts of polycaprolactone-modified hydroxyethyl acrylate (PLACCEL FA5), 0.02 parts of dibutyltin laurate, and 0.02 parts of hydroquinone monomethyl ether were charged. The mixture was maintained at 70° C. for 3 hours to complete the reaction, and 76.5 parts of toluene were added to obtain a urethane acrylate containing 50% by weight of solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825243B2
Source datasetuspto-grants-2004_11
ORD IDord-17ebe6446b3942bdafa6a6bbfa6ea1a3
Source noteuspto-grants-2004_11