Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Toluene 2,4-Diisocyanate | HCID 11443 | — |
| Reactant | 2-Hydroxyethyl acrylate | HCID 13165 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Product | Carbamic acid, ethyl ester | HCID 5641 | — |
| Product | Styrene | HCID 7501 | 50% |
Reaction Steps
A hydroxyl polyester having an acid number of 0.3 and a hydroxy number of 48.1 was prepared from 714 g (11.5 moles) of ethylene glycol and 1460 g (10 moles) of adipic acid in the conventional manner. 400 ppm of hydroquinone were added to this polyester to obtain a 50% styrene solution of the polyester. 4676 g (2 equivalents) of this solution were allowed to react with 248 g (2.85 equivalents) of tolylene diisocyanate and 116 g (1 mole) of hydroxylethyl acrylate at 65° C. or less for two hours. To the resulting reaction product were added dropwise over 1.5 hours 364 g of styrene and 2.7 g of dibutyltin dilaurate. The reaction was allowed to continue at 70° C. for further two hours until no NCO remained in the reaction system, thereby to obtain a 50% styrene solution of an unsaturated acrylic urethane (hereinafter called Acrylic Urethane I). The urethane was found to have a weight-average extension of molecular chain of 600 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-388ce604aa904bd5af9696c31d28cf64 |
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| Source note | uspto-grants-1983_06 |
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