Synthesis of Aminated Aromatic Imide Compounds
Publication: DE102013106983A1
Published: 2015-01-08
Family Size: 1
Granted: No
Simple SummaryContent extracted from patent full text and abstract with AI.
This patent describes a method for the oxidative amination of polycyclic aromatic imide compounds using copper catalysis. In simple terms, it provides a chemical process to efficiently attach amine groups to complex aromatic imide structures with the help of a copper-based catalyst.
Use CasesContent extracted from patent full text and abstract with AI.
- Synthesis of advanced organic materials for electronics, such as organic semiconductors or light-emitting diodes (OLEDs).
- Development of new pharmaceuticals by modifying aromatic imide scaffolds to improve biological activity or solubility.
- Production of specialty polymers with enhanced thermal or mechanical properties due to functionalized imide units.
- Manufacturing of dyes or pigments with improved stability and coloration characteristics.
BenefitsContent extracted from patent full text and abstract with AI.
- Enables efficient and selective introduction of amine groups into complex aromatic imide compounds.
- Utilizes copper catalysis, which is generally less expensive and potentially more environmentally friendly than using precious metal catalysts.
- Facilitates access to a wider range of functionalized imide compounds for advanced materials science and drug discovery.
- May offer improved yields, reaction speeds, and scalability compared to traditional methods of aromatic amine synthesis.
Technical Classifications (CPCs)
Main Classifications
Chemistry & Materials Science
Sub Classifications
Organic Chemistry
CPC Codes
C07D471/06
Inventors & Applicants
Inventors
Applicants
Univ Bonn
Patent Abstract
Die vorliegende Erfindung betrifft die oxidative Aminierung von mehrkernig-aromatischen Imidverbindungen mittels Kupferkatalyse.
Key Information
Publication No.
DE102013106983A1
Family ID
52106038
Publication Date
2015-01-08
Application No.
DE102013106983A
Application Date
2013-07-03
Priority Date
2013-07-03
Granted
No
Possible Cooperation
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