Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adipic Acid | HCID 196 | — |
| Reactant | Terephthalic Acid | HCID 7489 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Reactant | Neopentyl glycol | HCID 31344 | — |
| Reactant | Hexanediol | HCID 147023 | — |
| Reactant | Isophorone diisocyanate | HCID 169132 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Solvent | Hydroquinone | HCID 785 | — |
| Solvent | Styrene | HCID 7501 | — |
| Product | Carbamic acid, ethyl ester | HCID 5641 | — |
| Product | Styrene | HCID 7501 | 50% |
Reaction Steps
Apart from this, a hydroxyl polyester (hereinafter called Polyester J) having an acid number of 0.3 and a hydroxyl number of 60.4 was prepared from 767 g (6.5 moles) of hexanediol--1, 6, 520 g (5 moles) of neopentyl glycol, 498 g (3 moles) terephthalic acid, 730 g (5 moles) of adipic acid and 196 g (2 moles) of maleic anhydride. 1858 g (2 equivalents) of the polyester was dissolved in 2321 g of styrene containing 1.4 g of hydroquinone, and allowed to react with 333 g (3 equivalents) of isophorone diisocyanate at around 55° C. for three hours. 130 g (1 mole) of hydroxylethyl methacrylate containing 2.3 g of dibutyltin dilaurate were added dropwise to the reaction product while feeding air into the reaction system. The reaction was allowed to continue at 60° C. for further four hours until no NCO remained substantially in the system. The reaction product was then cooled with the addition of 30 g of a 50% styrene solution of Polyester J to obtain a 50% styrene solution of an unsaturated acrylic urethane (hereinafter called Acrylic Urethane K). This urethane was found to have a weight-average extension of molecular chain of 380 A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04390662 |
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| Source dataset | uspto-grants-1983_06 |
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| ORD ID | ord-eabf6154b46347f3907c35ef59d30f98 |
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| Source note | uspto-grants-1983_06 |
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