Synlett 2004(7): 1254-1258  
DOI: 10.1055/s-2004-825584
LETTER
© Georg Thieme Verlag Stuttgart · New York

CuI-Catalyzed Coupling Reactions of Aryl Iodides and Bromides with Thiols Promoted by Amino Acid Ligands

Wei Deng, Yan Zou, Ye-Feng Wang, Lei Liu*, Qing-Xiang Guo*
Deparment of Chemistry, University of Science and Technology of China, Hefei 230026, P. R. China
e-Mail: leiliu@chem.columbia.edu; e-Mail: qxguo@ustc.edu.cn;
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Publikationsverlauf

Received 1 March 2004
Publikationsdatum:
10. Mai 2004 (online)

Abstract

Novel mild conditions for the CuI-catalyzed coupling ­reactions of aryl iodides and bromides with aliphatic and aromatic thiols using amino acids as the ligand are reported.

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All the products are known compounds except for 1,4-bis(octylthio)benzene.

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1,4-Bis(octylthio)benzene: White solid. IR: 2954, 2921, 1465, 1113, 803 cm-1. 1H NMR (CDCl3, 300 MHz): δ = 7.23 (s, 4 H), 2.88 (t, J = 7.3 Hz, 4 H), 1.63 (m, J = 6.8 Hz, 4 H), 1.40-1.26 (br m, 20 H), 0.88 (t, J = 6.4 Hz, 6 H). 13C NMR (300 MHz, CDCl3): δ = 134.6, 129.8, 34.2, 32.0, 29.32, 29.29, 29.0, 22.8, 14.2. MS (EI): m/z (relative intensity): 366 (100), 254 (25), 142 (35). Anal. Calcd for C22H38S2: C, 72.06; H, 10.46. Found: C, 72.20; H, 10.58.