Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | 4-[1,1,1,3,3,3-Hexafluoro-2-(4-hydroxycyclohexyl)propan-2-yl]cyclohexan-1-ol | HCID 2782224 | — |
| Reactant | Isophorone DI-isocyanate | HCID 21298402 | — |
| Catalyst | 4-Methoxyphenol | HCID 9015 | — |
| Catalyst | Di-n-butyldilauryltin | HCID 9809426 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Urethane acrylate | HCID 21863578 | 821.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04788327 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-e0176e71a351451480f0d2f604d40f58 |
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| Source note | uspto-grants-1988_11 |
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