ADVERTISEMENT
2 /3 FREE ARTICLES LEFT THIS MONTH Remaining
Chemistry matters. Join us to get the news you need.

If you have an ACS member number, please enter it here so we can link this account to your membership. (optional)

ACS values your privacy. By submitting your information, you are gaining access to C&EN and subscribing to our weekly newsletter. We use the information you provide to make your reading experience better, and we will never sell your data to third party members.

ENJOY UNLIMITED ACCES TO C&EN

Synthesis

Systematic Synthesis Loads Up Aromatics

Chemists develop a general method for making hexaarylbenzenes and other highly substituted aromatic compounds

by Stephen K. Ritter
February 2, 2015 | APPEARED IN VOLUME 93, ISSUE 5

Benzene is the quintessential aromatic molecule and serves as an indispensable building block of pharmaceuticals, plastics, and more. Yet chemists have never gotten around to developing a general approach for substituting benzene with six different aryl groups, meaning that benzene’s structural diversity is far from being exhausted. Kenichiro Itami, Junichiro Yamaguchi, and coworkers of Nagoya University, in Japan, have decided to have a go at filling this void. By taking advantage of the richness of organic synthesis, the researchers created a programmed approach (shown) for preparing hexaarylbenzenes as well as multisubstituted naphthalenes and pyridines (Nat. Chem. 2015, DOI: 10.1038/nchem.2174). The team studied many synthetic methodologies and found that by starting with 3-methoxythiophene and using a combination of C–H activation, cross-coupling, and [4+2] cycloaddition reactions they can systematically prepare multisubstituted aromatics. Although the Nagoya chemists have made a variety of new compounds, they estimate that with the array of substituents at hand, more than 1 billion hexaarylbenzenes are still waiting to be made.

X

Article:

This article has been sent to the following recipient:

Comments
Robert Buntrock (February 6, 2015 10:52 AM)
The primary prep in Advanced Organic Chemistry Lab in Spring Quarter 1960 at the University of Minnesota was the comparatively prosaic but facile Diels Alder prep of hexaphenylbenzene from tetraphenylcyclopentadieneone and diphenylacetylene. We also prepared the bright purple ketone. We've come a long way ...

Leave A Comment

*Required to comment