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Solid Catalysts for Multistep Reactions: One- Pot Synthesis of 2,3-Dihydro-1,5-benzothiazepines with Solid Acid and Base Catalysts

机译:用于多体反应的固体催化剂:用固体酸和碱催化剂合成2,3-二氢-1,5-苯并噻嗪类化合物

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摘要

1,5-Benzothiazepines derivatives were obtained first by starting from 1,3-diphenylpropenone derivatives (chalcones) and 2-aminothiophenol by using aluminosilicate solid catalysts. However, diffusional limitations and the strong adsorption of products on the catalyst are deleterious for catalyst activity and life. Then a structured amorphous mesoporous catalyst with large pores and mild acidity that works at higher temperatures allowed us to obtain high conversions (99%) and selectivities (98%) of the desired product. A one-pot synthesis of 1,5-benzothiazepines that starts from benzaldehyde, acetophenone, and 2-aminothiophenol with 95% yield was performed by combining optimized solid base and acid catalysts in batch mode as well as in a continuous-flow reactor system. Much better conversion and selectivity as well as process intensification has been achieved with the structured mesoporous materials by avoiding intermediate and final neutralization and purification steps required in the synthesis reported previously that uses homogeneous catalysts.
机译:通过使用硅铝酸盐固体催化剂从1,3-二苯基酮衍生物(Chalcones)和2-氨基噻吩酚开始,首先获得1,5-苯并噻嗪类衍生物。然而,扩散限制和催化剂上的产品的强烈吸附对于催化剂活性和寿命有害。然后是具有大孔和温和酸度的结构化无定形介孔催化剂,其在较高温度下起作用,使我们获得高转化率(99%)和选择性(98%)所需产物。通过将优化的固体碱和酸催化剂与批量模式以及连续流动反应器系统组合,通过将优化的固体碱和酸催化剂以及连续流动反应器系统组合来进行1,5-苯甲苯二酚的1,5-苯酚和2-氨基酚酚的单钾合成。通过避免使用均匀催化剂所需的合成中所需的中间和最终中和和纯化步骤,通过结构化的介孔材料实现了更好的转化和选择性以及过程强化。

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