Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylolpropane | HCID 6510 | — |
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | 1,3-Bis(isocyanatomethyl)benzene | HCID 19262 | — |
| Reactant | Bis(isocyanatomethyl)benzene | HCID 3035160 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Urethane acrylate | HCID 21863578 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825243B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-17ebe6446b3942bdafa6a6bbfa6ea1a3 |
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| Source note | uspto-grants-2004_11 |
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