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以甲酸作为CO来源,磁性可回收钯-催化芳基碘甲酰化制备芳醛的一种实用方法 2021-12-14

Synthesis 2021; 53(11): 1962-1970
DOI: 10.1055/s-0040-1706621

Paper

Shengyong YouRongli ZhangMingzhong Cai

A Magnetically Recyclable Palladium-Catalyzed Formylation of Aryl Iodides with Formic Acid as CO Source: A Practical Access to Aromatic Aldehydes

以甲酸作为CO来源,磁性可回收钯-催化芳基碘甲酰化制备芳醛的一种实用方法

采用膦氧双齿配体修饰磁性纳米粒子锚定钯(II)复合物[2P-Fe3O4@SiO2-Pd(OAc)2]为催化剂,在无 CO 气体条件下,对芳基碘进行磁性可回收钯-催化甲酰化,以中等到极高的收率得到各种不同的芳醛。该策略中,采用甲酸为 CO 来源和氢供体,采用碘和 PPh3 为活化剂。锚定钯催化剂可通过简单的方法制得,并可采用外部磁场轻松回收,可重复使用 9 次而不会发生任何明显的催化活性损失。

A magnetically recyclable palladium-catalyzed formylation of aryl iodides under CO gas-free conditions has been developed by using a bidentate phosphine ligand-modified magnetic nanoparticles-anchored­ palladium(II) complex [2P-Fe3O4@SiO2-Pd(OAc)2] as catalyst, yielding a wide variety of aromatic aldehydes in moderate to excellent yields. Here, formic acid was employed as both the CO source and the hydrogen donor with iodine and PPh3 as the activators. This immobilized palladium catalyst can be obtained via a simple preparative procedure and can be facilely recovered simply by using an external magnetic field, and reused at least 9 times without any apparent loss of catalytic activity.

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Synthesis

3.157  ↑18%

Impact Factor 2020

本刊为国际性论文全文期刊,致力于推动合成化学科学的发展。它涵盖了所有涉及合成有机化学领域,包括催化、有机金属、医药、生物学和光化学,也包括其他相关学科。SYNTHESIS上的内容翔实地记载了实验流程,完整地描述了所有重要新产品,提供了可靠的研究成果和科学原始数据。