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 liquid phase aeration method. Thus, the air in a 300 ml four-necked flask similar to the one used in Example 5 was replaced with nitrogen and, then, the flask was charged with 98 g of maleic anhydride, 300 ppm of p-tert-butylcatechol by way of auxiliary polymerization inhibitor and 800 ppm of dilauryl thiodipropionate by way of auxiliary polymerization inhibitor and the charge was melted at 60° C. Then, the internal atmosphere of the reaction system was replaced with nitrogen gas, and thereafter nitrogen gas containing 1 volume % of oxygen was passed into the reaction mixture at a rate of 5 ml/min throughout the reaction. 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 60° C. for 4 hours. Major portion of unreactive fractions was distilled off from the reaction mixture in the course of reaction. Thereafter, the reaction mixture was treated in the same manner as in Example 5 to give 164 g of 3Me--THPA. The investigation revealed no gels in the product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05237074 |
|---|
| Quelldatensatz | uspto-grants-1993_08 |
|---|
| ORD ID | ord-a2b09e0aab0147408fda825908cb4e7e |
|---|
| Quellennotiz | uspto-grants-1993_08 |
|---|