Synthesis 2007(19): 2944-2946  
DOI: 10.1055/s-2007-983890
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Organosilatranes via Rhodium(I)-Catalyzed Silylation of Organic Iodides with Hydrosilatrane

Miki Murata*, Hiroyuki Yamasaki, Kota Uogishi, Shinji Watanabe, Yuzuru Masuda
Department of Materials Science, Kitami Institute of Technology, 165 Koen-cho, Kitami, Hokkaido 090-8507, Japan
Fax: +81(157)264973; e-Mail: muratamk@mail.kitami-it.ac.jp;
Further Information

Publication History

Received 6 June 2007
Publication Date:
11 September 2007 (online)

Abstract

The silylation of aryl and alkenyl iodides with hydro­silatrane in the presence of a rhodium(I) catalyst and DABCO provides the corresponding organosilatranes in good yield. The same catalyst system also enables the related coupling of hydrogermatrane.

6

Kishida, E.; Saiki, T.; Ishiyama, T.; Miyaura, N. The 53rd Symposium on Organometallic Chemistry; Osaka, Japan, September 8-9, 2006; Abstract PB253.

10

The results of the silylation of ethyl 4-iodobenzoate with hydrosilatrane (1) in the presence of [Rh(cod)(MeCN)2]BF4 and DABCO in selected solvents are as follows [% NMR yield (% conversion)]: DMF, 63 (100); DMSO, 0 (100); MeCN, 0 (100); dioxane, 38 (100); DCE, 0 (8); toluene, trace (27).

13

To some extent, a plausible mechanism for the case of triethoxysilane, proposed by us (see ref. 8b), would refer to the present situation.