Hwu Jih Ru, Bohara Khagendra Prasad, Roy Animesh, Huang Wen-Chieh, Hwang Kuo-Chu, Lin Chun-Cheng, Chuang Kao Shu, Lin Shu-Yu, Tsay Shwu-Chen
Department of Chemistry and Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University, Hsinchu 30013, Taiwan.
Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli County 350401, Taiwan.
J Org Chem. 2025 Apr 25;90(16):5343-5348. doi: 10.1021/acs.joc.4c02340. Epub 2025 Apr 16.
An innovative method was developed for the performance of aldol additions in an irreversible fashion by the use of calcium metal impregnated silica gel (Ca@SiO) as a remarkable reducing reagent. In this approach, Ca@SiO drove the reaction forward, prevented reversibility, and ensured the formation of the desired products. Thus, in the presence of Ca@SiO (3.0 equiv), aldehydes (1.0 equiv) condensed with ketones (1.0 equiv) in 2-MeTHF to yield α,β-unsaturated enones in 71-90% yields at 25 °C. Additionally, a domino reaction involving successive aldol addition, dehydration, and Michael addition was developed for the preparation of 1,5-diketones. Accordingly, when aldehydes (1.0 equiv) were allowed to react with ketones (2.2 equiv) and Ca@SiO(4.0 equiv), 1,5-diketones were produced in 67-88% yields. These reactions involved radical processes, where Ca@SiO abstracted two α hydrogen atoms from ketones and the oxygen atom from aldehydes to form CaH@SiO and CaO@SiO, respectively. These species were confirmed by powder X-ray diffraction analysis. The resultant impregnated silica gel species were solid and insoluble in the reaction mixtures, which made the addition reactions irreversible. This method represents a significant advancement in aldol condensation reactions and offers the advantages of both atom economy and atom efficiency.
通过使用负载钙金属的硅胶(Ca@SiO)作为一种卓越的还原剂,开发了一种以不可逆方式进行羟醛加成反应的创新方法。在这种方法中,Ca@SiO推动反应向前进行,防止反应可逆,并确保所需产物的形成。因此,在Ca@SiO(3.0当量)存在下,醛(1.0当量)与酮(1.0当量)在2-甲基四氢呋喃中缩合,于25℃下以71-90%的产率生成α,β-不饱和烯酮。此外,还开发了一种涉及连续羟醛加成、脱水和迈克尔加成的多米诺反应来制备1,5-二酮。相应地,当醛(1.0当量)与酮(2.2当量)和Ca@SiO(4.0当量)反应时,1,5-二酮的产率为67-88%。这些反应涉及自由基过程,其中Ca@SiO分别从酮中夺取两个α氢原子和从醛中夺取氧原子,形成CaH@SiO和CaO@SiO。这些物质通过粉末X射线衍射分析得到证实。所得的负载硅胶物质为固体,不溶于反应混合物,这使得加成反应不可逆。该方法代表了羟醛缩合反应的重大进展,并具有原子经济性和原子效率的优点。