Synlett 2017; 28(07): 835-840
DOI: 10.1055/s-0036-1588930
letter
© Georg Thieme Verlag Stuttgart · New York

Ligandless Palladium-Catalyzed Reductive Carbonylation of Aryl Iodides under Ambient Conditions

Wei Han*
a   Jiangsu Key Laboratory of Biofunctional Materials, Key Laboratory of Applied Photochemistry, School of Chemistry and Materials Science, Nanjing Normal University, Wenyuan Road NO.1, Nanjing 210023, P. R. of China   Email: hanwei@njnu.edu.cn
b   Jiangsu Collaborative Innovation Center of Biomedical Functional Materials, Nanjing 210023, P. R. of China
,
Binbin Liu
a   Jiangsu Key Laboratory of Biofunctional Materials, Key Laboratory of Applied Photochemistry, School of Chemistry and Materials Science, Nanjing Normal University, Wenyuan Road NO.1, Nanjing 210023, P. R. of China   Email: hanwei@njnu.edu.cn
,
Junjie Chen
a   Jiangsu Key Laboratory of Biofunctional Materials, Key Laboratory of Applied Photochemistry, School of Chemistry and Materials Science, Nanjing Normal University, Wenyuan Road NO.1, Nanjing 210023, P. R. of China   Email: hanwei@njnu.edu.cn
,
Qing Zhou
a   Jiangsu Key Laboratory of Biofunctional Materials, Key Laboratory of Applied Photochemistry, School of Chemistry and Materials Science, Nanjing Normal University, Wenyuan Road NO.1, Nanjing 210023, P. R. of China   Email: hanwei@njnu.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 26 October 2016

Accepted after revision: 13 December 2016

Publication Date:
12 January 2017 (online)


Abstract

Ligandless palladium-catalyzed reductive carbonylation of aryl iodides for the synthesis of aromatic aldehydes has been developed. This carbonylation process proceeded effectively even under ambient temperature and pressure. In addition, this method enables successive reductive carbonylation of diiodobenzenes to furnish dialdehydes in satisfactory yields. Finally, the nature of the active catalytic species is discussed.

Supporting Information