Rh-Catalysed Trifluoromethylation of Ketene Silyl Acetal
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- YUKI Takashi
- Faculty of Pharmaceutical Sciences, Setsunan University
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- YAMAGUCHI Ryoji
- Faculty of Pharmaceutical Sciences, Setsunan University
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- SATO Kazuyuki
- Faculty of Pharmaceutical Sciences, Setsunan University
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- TARUI Atsushi
- Faculty of Pharmaceutical Sciences, Setsunan University
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- OMOTE Masaaki
- Faculty of Pharmaceutical Sciences, Setsunan University
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- ANDO Akira
- Faculty of Pharmaceutical Sciences, Setsunan University
Bibliographic Information
- Other Title
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- ケテンシリルアセタールを用いた Rh 触媒 α-CF<SUB>3</SUB> 化反応の開発
Description
We already reported a perfluoroalkylation using ketone silyl enol ethers in the presence of Wilkinson's catalyst to give α-perfluoroalkylated ketones in moderate yields. However, using some perfluoroalkyl halides such as CF3I or C4F9I which have lower boiling points lead to the lower yields, because the reaction needed to heat at 130ºC. As solve the problem, we examined the various conditions of α-trifluoromethylation, and found that the addition of Et2Zn into the reaction mixture improved the yield of α-CF3 ketones. Furthermore, this condition could apply not only ketone silyl enol ethers but also ketene silyl acetals to give α-CF3 esters in moderate to good yields.
Journal
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- Proceedings of the Symposium on Progress in Organic Reactions and Syntheses
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Proceedings of the Symposium on Progress in Organic Reactions and Syntheses 33 (0), 90-90, 2007
Division of Organic Chemistry, The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390282680610172160
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- NII Article ID
- 130006995550
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed