Interdisciplinary Research Center for Catalytic Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8565, Japan.
Org Biomol Chem. 2021 Feb 11;19(5):1115-1121. doi: 10.1039/d0ob02213f.
The oxidation of alcohols to aldehydes is a powerful reaction pathway for obtaining valuable fine chemicals used in pharmaceuticals and biologically active compounds. Although many oxidants can oxidize alcohols, only a few hydrogen peroxide oxidations can be employed to continuously synthesize aldehydes in high yields using a liquid-liquid two-phase flow reactor, despite the possibility of the application toward a safe and rapid multi-step synthesis. We herein report the continuous flow synthesis of (E)-cinnamaldehyde from (E)-cinnamyl alcohol in 95%-98% yields with 99% selectivity for over 5 days by the selective oxidation of hydrogen peroxide using a catalyst column in which Pt is dispersed in SiO2. The active species for the developed selective oxidation is found to be zero-valent Pt(0) from the X-ray photoelectron spectroscopy measurements of the Pt surface before and after the oxidation. Using Pt black diluted with SiO2 as a catalyst to retain the Pt(0) species with the optimal substrate and H2O2 introduction rate not only enhances the catalytic activity but also maintains the activity during the flow reaction. Optimizing the contact time of the substrate with Pt and H2O2 using a flow reactor is important to proceed with the selective oxidation to prevent the catalytic H2O2 decomposition.
醇氧化为醛是获得用于制药和生物活性化合物的有价值精细化学品的有力反应途径。尽管许多氧化剂可以氧化醇,但只有少数过氧化氢氧化可以在使用液-液两相流反应器的情况下以高产率连续合成醛,尽管有可能应用于安全快速的多步合成。在此,我们报告了在催化剂柱中使用 Pt 分散在 SiO2 中的方法,通过过氧化氢的选择性氧化,以 95%-98%的收率和 99%的选择性连续合成(E)-肉桂醛,从(E)-肉桂醇中连续合成(E)-肉桂醛,超过 5 天。从氧化前后 Pt 表面的 X 射线光电子能谱测量结果发现,用于开发的选择性氧化的活性物质是零价 Pt(0)。使用 Pt 黑和 SiO2 稀释作为催化剂,保留具有最佳底物和 H2O2 引入率的 Pt(0)物种,不仅提高了催化活性,而且在流动反应过程中保持了活性。使用流动反应器优化底物与 Pt 和 H2O2 的接触时间对于进行选择性氧化以防止催化 H2O2 分解很重要。