Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adipic Acid | HCID 196 | — |
| Reactant | Trimethylolpropane | HCID 6510 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 2-ethylhexanoic acid tin(II) salt | HCID 9318 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | Hexanediol | HCID 147023 | — |
| Reactant | Diisocyanatotoluene | HCID 12905475 | — |
| Reactant | Isophorone DI-isocyanate | HCID 21298402 | — |
| Product | Urethane acrylate | HCID 21863578 | — |
Reaction Steps
661.9 g of the ethylene oxide polyether started from trimethylolpropane esterified with 2 mol acrylic acid (12 mol ethylene oxide per mol trimethylolpropane) and 164.4 g of a polyester polyol from hexanediol and adipic acid (OH number 314, equivalent weight 178.5 g), 1.0 g 2,6-di-tert-butyl-4-methyl-phenol and 1.0 g tin octoate were initially introduced into the reaction vessel. 148.8 g Desmodur® T80 (toluylene diisocyanate, commercial product of Bayer AG, Leverkusen) were metered in at 50 to 60° C. After a further 5 h 31.6 g isophorone-diisocyanate were metered in. The reaction was carried out at 60° C. for a further 5 h and 74.0 g of the ethylene oxide polyether started from trimethylolpropane esterified with 2 mol acrylic acid (12 mol ethylene oxide per mol trimethylolpropane) were then added. The reaction was subsequently carried out at 60° C. until the NCO content of the solution was less than 0.10 wt. %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465539B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-a94cf400ad4f479eaaee61752ae937bd |
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| Source note | uspto-grants-2002_10 |
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