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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 868690Erstellt: 24. Oktober 2026

Phosphoric Acid → 1H-Pyrrole-2,5-dione, 1-dodecyl-

https://huagongshe.com/de/reaction/868690

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphoric AcidHCID 1004—
EduktMaleic AnhydrideHCID 7923—
EduktDodecylamineHCID 13583—
Edukt2-Methoxy-1,4-benzoquinoneHCID 76146—
KatalysatorZinc AcetateHCID 11192—
LösungsmittelTetralinHCID 8404—
Produkt1H-Pyrrole-2,5-dione, 1-dodecyl-HCID 87191—

Reaktionsbedingungen

Temperatur210 °C

Reaktionsschritte

The same reactor as used in Example 7 was adopted. In this reactor, a solution of 120 g of maleic anhydride in 360 g of tetrahydronaphthalene was placed. Then, a solution of 220 g of dodecylamine and 1760 g of tetrahydronaphthalene was added thereto at 40° C. over a period of 120 minutes. After the addition was completed, the resultant mixture and 65.4 g of ortho-phosphoric acid (purity 89% by weight), 1.344 g of methoxybenzoquinone, and 0.1 g of zinc acetate added thereto were heated at 210° C. for one hour to effect reaction. Thereafter, the resultant reaction mixture was cooled to 30° C. and separated into a water layer and a tetrahydronaphthalene layer. The tetrahydronaphthalene layer was distilled to expel tetrahydronaphthalene. Consequently, there was obtained 285 g of slightly impure N-dodecyl maleimide. It was found to have purity of 92.3% by weight, indicating the yield thereof to be 83.5 mol % based on dodecylamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04780546
Quelldatensatzuspto-grants-1988_10
ORD IDord-a656e95f3f9749a89d4dce64cc03a074
Quellennotizuspto-grants-1988_10