Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, People’s Republic of China.
J Am Chem Soc. 2012 Mar 7;134(9):4258-63. doi: 10.1021/ja210361z. Epub 2012 Feb 22.
Decarboxylative halogenation of carboxylic acids, the Hunsdiecker reaction, is one of the fundamental functional group transformations in organic chemistry. As the initial method requires the preparations of strictly anhydrous silver carboxylates, several modifications have been developed to simplify the procedures. However, these methods suffer from the use of highly toxic reagents, harsh reaction conditions, or limited scope of application. In addition, none is catalytic for aliphatic carboxylic acids. In this Article, we report the first catalytic Hunsdiecker reaction of aliphatic carboxylic acids. Thus, with the catalysis of Ag(Phen)(2)OTf, the reactions of carboxylic acids with t-butyl hypochlorite afforded the corresponding chlorodecarboxylation products in high yields under mild conditions. This method is not only efficient and general, but also chemoselective. Moreover, it exhibits remarkable functional group compatibility, making it of more practical value in organic synthesis. The mechanism of single electron transfer followed by chlorine atom transfer is proposed for the catalytic chlorodecarboxylation.
脱羧卤化羧酸,即 Hunsdiecker 反应,是有机化学中基本的官能团转化之一。由于最初的方法需要严格无水的银羧酸盐的制备,因此已经开发了几种改进方法来简化步骤。然而,这些方法存在使用剧毒试剂、苛刻的反应条件或应用范围有限等问题。此外,它们都不能催化脂肪族羧酸。在本文中,我们报道了首例脂肪族羧酸的催化 Hunsdiecker 反应。因此,在 Phen-Ag(2+)OTf 的催化下,羧酸与叔丁基次氯酸盐的反应在温和条件下以高产率得到相应的脱羧氯代产物。该方法不仅高效、通用,而且具有化学选择性。此外,它表现出显著的官能团相容性,使其在有机合成中具有更高的实用价值。提出了单电子转移后氯原子转移的催化脱羧氯代反应机理。