Understanding the Synthesis and Properties of 9-(4-Bromophenyl)-3,6-Di-tert-butyl-9H-carbazole
For professionals working with advanced organic materials, understanding the synthesis and intrinsic properties of key intermediates is fundamental. 9-(4-Bromophenyl)-3,6-Di-tert-butyl-9H-carbazole (CAS: 601454-33-5) is a notable example, frequently utilized in the development of organic electronic devices, particularly OLEDs, and as a versatile building block in sophisticated organic synthesis. This article aims to provide a focused overview of its preparation and characteristics, offering valuable information for procurement specialists and research scientists alike.
The primary synthesis route for 9-(4-Bromophenyl)-3,6-Di-tert-butyl-9H-carbazole typically involves palladium-catalyzed cross-coupling reactions. A common method combines 3,6-di-tert-butyl-9H-carbazole with a 4-bromophenyl derivative, often under Buchwald-Hartwig amination conditions. This process leverages the nucleophilic character of the carbazole nitrogen to form a new carbon-nitrogen bond. The reaction requires careful control of catalysts, bases, solvents, and temperature to achieve optimal yields, which are reported to be around 58% under specific conditions. Ensuring high purity post-synthesis, often through recrystallization or chromatography, is crucial for its subsequent applications.
The molecular structure of 9-(4-Bromophenyl)-3,6-Di-tert-butyl-9H-carbazole confers several advantageous properties. The bulky tert-butyl groups at the 3 and 6 positions significantly enhance its solubility in common organic solvents and improve its thermal stability, raising its glass transition temperature. These groups also play a role in reducing intermolecular interactions, which can positively impact photophysical properties in solid-state applications. The presence of the bromine atom on the phenyl ring makes it an excellent substrate for further chemical modifications, such as Suzuki-Miyaura or Sonogashira couplings, allowing for the construction of larger, more complex molecular frameworks required for advanced materials.
For those looking to buy this compound, understanding these synthesis and property aspects is key to selecting the right supplier. Manufacturers who can consistently deliver this intermediate with high purity and provide detailed technical specifications are invaluable partners for research and industrial production.
Perspectives & Insights
Data Seeker X
“The presence of the bromine atom on the phenyl ring makes it an excellent substrate for further chemical modifications, such as Suzuki-Miyaura or Sonogashira couplings, allowing for the construction of larger, more complex molecular frameworks required for advanced materials.”
Chem Reader AI
“For those looking to buy this compound, understanding these synthesis and property aspects is key to selecting the right supplier.”
Agile Vision 2025
“Manufacturers who can consistently deliver this intermediate with high purity and provide detailed technical specifications are invaluable partners for research and industrial production.”