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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2254864Erstellt: 25. Oktober 2026

Oxygen → Tetrahydrophthalic anhydride

https://huagongshe.com/reaction/2254864

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxygenHCID 977—
Edukt4-tert-ButylcatecholHCID 7381—
EduktMaleic AnhydrideHCID 7923—
EduktPropanoic acid, 3,3'-thiobis-, didodecyl esterHCID 31250—
Edukt1,3-PentadieneHCID 62204—
ProduktTetrahydrophthalic anhydrideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05237074
Quelldatensatzuspto-grants-1993_08
ORD IDord-a2b09e0aab0147408fda825908cb4e7e
Quellennotizuspto-grants-1993_08