Heck Reaction Goes Silyl | Chemical & Engineering News
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Web Date: March 26, 2012

Heck Reaction Goes Silyl

ACS Meeting News: Ligand enables silicon variant of familiar palladium-catalyzed chemistry
Department: Science & Technology
News Channels: Materials SCENE
Keywords: Catalysis, organometallic chemistry, silicon, palladium, Heck reaction
The silyl-Heck reaction converts carbon-hydrogen bonds to carbon-silicon bonds.
Reaction scheme shows the silyl-Heck reaction converting carbon-hydrogen bonds to carbon-silicon bonds.
The silyl-Heck reaction converts carbon-hydrogen bonds to carbon-silicon bonds.

By designing a “goldilocks” catalyst—one with just the right balance of size and electron-donating properties—University of Delaware chemists have added a new reaction to the tool kit for forming carbon-silicon bonds.

The process converts alkenes, which are easily accessible starting materials, to vinylsilanes and allylsilanes, reagents with applications in several branches of synthesis. Donald A. Watson, who led the research, presented the work on Sunday in the Division of Organic Chemistry at the ACS national meeting in San Diego.

Chemists already have ways of obtaining allylsilanes and vinylsilanes. “But they’re not easy to make and they tend to require harsh conditions,” Watson told C&EN. Building on other labs’ work, Watson, graduate students Jesse R. McAtee and Sara E. S. Martin, and colleagues set out to develop a mild, palladium-catalyzed reaction that would convert the C–H bond of an alkene to a C–Si bond, analogous to the Nobel Prize-winning Heck reaction, which converts those C–H bonds to C–C bonds.

The group’s first attempts didn’t work, but they eventually realized the problem was a bulky ligand on their catalyst. It provided much-needed electron donation, but it just got in the way, preventing the reaction, Watson explained. Eventually, his group found a ligand that was not too big and not too small: tert-butyldiphenylphosphine. With their ligand now just right, they modified the reaction conditions to use the silane source chlorotrimethylsilane in place of iodotrimethylsilane because the former sells for a fraction of the price (Angew. Chem. Int. Ed., DOI: 10.1002/anie.201200060).

Scott E. Denmark, an expert in organosilicon chemistry at the University of Illinois, Urbana-Champaign, told C&EN what’s most interesting about the new method is that it generates a trimethylsilylmetal intermediate that could be broadly useful. Although the compounds the team reported in the paper can be made in other ways, “the authors have an opportunity for making an impact on other less readily available silanes,” he said.

It’s possible the method could even be applied to polymers such as silicones, added Michael A. Brook, an expert in materials chemistry of silicon at McMaster University, in Ontario.

In San Diego, Watson mentioned that his team is working toward an X-ray structure of their trimethylsilylmetal intermediate, which he says will help them further optimize reaction conditions.

“This is a creative piece of work,” said Edward A. Anderson, who studies vinylsilanes at Oxford University. He cautions that the reaction’s current need for excess silane might limit its application to highly functionalized substrates. However, the Delaware team’s search for the best ligand “showed great insight,” he added. “It is surprising that this reaction has not been developed before now.”

C&EN Covers The ACS National Meeting

Want the scoop on the ACS meeting in San Diego? Check out C&EN Picks, a series of videos that spotlight sessions selected by C&EN staff. Reporters also fan out across the meeting to bring you news coverage. Find it all collected at C&EN’s meeting page, cenatacs.tumblr.com.

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