Synfacts 2009(9): 1027-1027  
DOI: 10.1055/s-0029-1217764
Metal-Mediated Synthesis
© Georg Thieme Verlag Stuttgart ˙ New York

Direct C-H Arylation of Benzene, Naphthalene, and Pyridine

Contributor(s): Paul Knochel, Tobias Thaler
O. Kobayashi, D. Uraguchi, T. Yamakawa*
Sagami Chemical Research Center, Ayase, Japan
Further Information

Publication History

Publication Date:
21 August 2009 (online)

Significance

Direct C-H arylation of benzene, naphthalene, and pyridine was achieved using Cp2Ni as catalyst in the presence of KOt-Bu and Et3B or Ph3P (for arylation of pyridine). The best yields were obtained with aryl bromides as electrophiles. Arylations of naphthalene proceeded with a preference for the 1-arylated product. For pyridine, positions 2 and 3 were preferentially arylated.