Continuous synthesis of homoallylic ketones via ketal-Claisen rearrangement using solid-acid catalysts

被引:1
|
作者
Kobayashi, Kwihwan [1 ]
Negoro, Chie [1 ]
Takaishi, Junko [1 ]
Masuda, Koichiro [1 ]
Kobayashi, Shu [1 ,2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol Cent 5, Interdisciplinary Res Ctr Catalyt Chem, Higashi 1-1-1, Tsukuba, Ibaraki 3058565, Japan
[2] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1110033, Japan
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 07期
关键词
ONE-POT SYNTHESIS; ALLYLIC ALKYLATION; GAMMA; DELTA-UNSATURATED KETONES; HETEROGENEOUS CATALYSIS; SULFATED ZIRCONIA; ENOL ETHERS; IRMS-TPD; EFFICIENT; PERFORMANCE; ALCOHOLS;
D O I
10.1039/d3qo01889j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Homoallylic ketones are useful intermediates for the synthesis of various compounds, such as drugs and natural products. However, the currently available fabrication methods for homoallylic ketones are environmentally unfriendly and tedious. We herein describe a continuous synthesis of homoallylic ketones from allylic alcohols and dimethyl ketals via ketal-Claisen rearrangement using a column-type flow reactor and a solid-acid catalyst. We have shown that the flow of N-2 gas accompanying the reaction solution improved the flow ketal-Claisen rearrangement. Long-term operation (150 h) of the flow ketal-Claisen rearrangement using a column packed with TMEDA-treated SO3H-ZrO2 has been successfully achieved with over 70% yield of homoallylic ketones. We believe that our proposed method could prove highly useful in the synthesis of homoallylic ketones.
引用
收藏
页码:1990 / 1995
页数:6
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