Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methoxyphenol | HCID 9015 | — |
| Edukt | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| Edukt | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Edukt | 2-Hydroxypropyl acrylate | HCID 61249 | — |
| Edukt | Di-n-butyl diacetoxy tin | HCID 9798523 | — |
| Produkt | Urethane acrylate | HCID 21863578 | — |
Reaktionsschritte
260 g (2 mol) of 2-hydroxypropyl acrylate (molecular weight 130) was placed in a flask equipped with a stirring blade, and with constant stirring, 174 g (1 mol) of TDI (2,4-tolylene diisocyanate) was added dropwise, with care taken over the generated heat, and the temperature was raised to 70° C. 1 g of dibutyl tin diacetate, 0.2 g of hydroquinone monomethyl ether and 1 g of 2,6-di-t-butyl-4-methylphenol were then added. Reaction was allowed to proceed at this temperature for 7 hours, and once the disappearance of NCO absorption had been confirmed via an infrared absorption spectrum, the reaction mixture was removed, yielding a urethane acrylate (A-X) as the radical polymerizable oligomer (A). The number average molecular weight of the synthesized urethane acrylate (A-X) was 434.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06853788B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-fcd592e6641c4edf9c1358088911e541 |
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| Quellennotiz | uspto-grants-2005_02 |
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