Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Oxygen | HCID 977 | — |
| Edukt | 4-tert-Butylcatechol | HCID 7381 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Propanoic acid, 3,3'-thiobis-, didodecyl ester | HCID 31250 | — |
| Edukt | 1,3-Pentadiene | HCID 62204 | — |
| Produkt | Tetrahydrophthalic anhydride | HCID 6810 | — |
Reaktionsschritte
3Me--THPA was produced by the gas phase aeration method. Thus, the air in a 300-ml four-necked flask equipped with a stirrer, thermometer, condenser, a dropping funnel for feeding crude trans-1,3-pentadiene, and an unreactive fraction recovery vessel was replaced with nitrogen and, then, the flask was charged with 98 g of maleic anhydride, 500 ppm of p-tert-butylcatechol by way of radical polymerization inhibitor and 1000 ppm of dilauryl thiodipropionate as auxiliary polymerization inhibitor. The charge was melted at 50° to 55° C. and after the internal atmosphere was replaced with nitrogen gas, nitrogen gas containing 4% of oxygen was passed through the gas phase at a rate of 10 ml/min throughout the reaction period. Under this atmosphere, 374 g of crude trans-1,3-pentadiene of the same composition as that used in Example 1 was continuously added at 50° to 55° C. over a period of 4 hours. During the reaction, major portion of unreactive fractions was distilled off from the reaction system. After completion of addition, the reaction was conducted at 70° C. for 30 minutes. After completion of the reaction, the reaction mixture was distilled at 85° C. under atmospheric pressure and, then, under reduced pressure to remove the volatile fraction. In this manner, 164 g of 3Me--THPA was obtained. The investigation revealed no gels in the product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05237074 |
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| Quelldatensatz | uspto-grants-1993_08 |
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| ORD ID | ord-4b050eb4c3be4500bf9d93c525f53888 |
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| Quellennotiz | uspto-grants-1993_08 |
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