Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Octanol | HCID 957 | — |
| Edukt | Pyromellitic Acid | HCID 6961 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | Tetraoctyl pyromellitate | HCID 21895707 | 209% |
Reaktionsschritte
To a 2-liter four necked flask equipped with Dean Stark apparatus, 218 g of anhydrous pyromellitic acid, 650 g of n-octanol, 0.2 g of titanium tetraisopropoxide and 300 cc of xylene were added and reacted with stirring at 160 degrees C. for 4 hours under nitrogen stream while distilling water. Subsequently, washing by saturated brine and washing by 0.1 N aqueous sodium hydroxide were respectively conducted three times, followed by being dried by anhydrous magnesium sulfate. After magnesium sulfate was filtered, unreacted alcohol was distilled under reduced pressure to obtain 630 g of tetraoctyl pyromellitate. Tetraoctyl pyromellitate, regarded as Comparative Example 3, was similarly measured with respect to the properties.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754019B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-0c7ffbe529c247c1ac5f07b5d68037c1 |
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| Quellennotiz | uspto-grants-2014_06 |
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