Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | Dimethylolpropionic acid | HCID 78501 | — |
| Reactant | Isophorone diisocyanate | HCID 169132 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Reactant | HCID 19351831 | HCID 19351831 | — |
| Product | Urethane acrylate | HCID 21863578 | — |
Reaction Steps
In a reaction vessel equipped with a stirrer, a thermometer and a condenser, 3750 g (3 mol) of polycaprolactonediol (PLACCEL212, manufactured by DAICEL CHEMICAL INDUSTRIES, LTD.) having a molecular weight of 1250 as the polymer polyol, 402 g (3 mol) of dimethylolpropionic acid as the dihydroxyl compound having a carboxyl group, 1554 g (7 mol) of isophorone diisocyanate as the polyisocyanate, 238 g (2.05 mol) of 2-hydroxyethyl acrylate as the (meth)acrylate, and p-methoxyphenol and di-t-butyl-hydroxytoluene (1.0 g each) were charged. The mixture was heated to 60° C. while stirring, and after heating was stopped, 1.6 g of dibutyltin dilaurate was added. When the temperature in the reaction vessel began to decrease, the mixture was heated again and was continuously stirred at 80° C. After confirming by an infrared absorption spectrum that an absorption spectrum (2280 cm−1) of an isocyanate group disappeared, the reaction was stopped to obtain a urethane acrylate compound as a viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06818382B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-f60e362f2a5745608536a2d7ec720081 |
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| Source note | uspto-grants-2004_11 |
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