Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acrylic Acid | HCID 6581 | — |
| Edukt | Succinic anhydride | HCID 7922 | — |
| Edukt | Hexamethylene diisocyanate | HCID 13192 | — |
| Edukt | bisphenol A bis-glycidyl ether | HCID 20266794 | — |
| Katalysator | 4-Methoxyphenol | HCID 9015 | — |
| Katalysator | Zinc Caprylate | HCID 11180 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-tert-Butylanthracene-9,10-dione | HCID 14274944 | — |
Reaktionsschritte
968 g of the reaction product of bisphenol A-bis-glycidyl ether and acrylic acid (containing 3.7 gram equivalents of OH) described in Example 1 were dissolved in 850 g of methylene chloride, followed by the addition of 0.6 ml of a concentrated zinc octoate solution and another 0.5 g of p-methoxy phenol. 168 g of hexamethylene diisocyanate (2 gram equivalents of NCO) were then added dropwise while the solution was boiled under reflux. After 24 hours' refluxing, an NCO-content of 0.5% was determined and 128 g of succinic acid anhydride (1.28 gram equivalents of anhydride) were added to the boiling solution. After another 12 hours, a clear solution was obtained to which 25.8 g of tert.-butyl anthraquinone (photoinitiator) were added, and the solution was left to cool.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04162274 |
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| Quelldatensatz | uspto-grants-1979_07 |
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| ORD ID | ord-cb0dc02ef8964e8a93ebf5512b9d572a |
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| Quellennotiz | uspto-grants-1979_07 |
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