Liu Yashuai, Yuan Yutong, He Jing, Han Sheng, Liu Yan
Basic Sciences Department, Shanxi Agricultural University Jinzhong 030800 P. R. China
School of Chemistry and Chemical Engineering, The Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, Shihezi University Shihezi City 832004 China
RSC Adv. 2024 Sep 19;14(41):29891-29895. doi: 10.1039/d4ra05383d. eCollection 2024 Sep 18.
An iodophor-catalyzed sulfenylation of indoles using sulfonyl hydrazides as sulfur source to synthesize 3-sulfenylindoles in aqueous phase has been achieved. Notably, iodophor as catalyst and solvent is inexpensive, commercially available and no innocuous to the environment. The method is also easy to operate. Moreover, the synthetic strategy features a wide range of substrates with excellent tolerance to diverse functional groups. A plausible mechanism for the iodophor-mediated 3-sulfenylation of indoles with sulfonyl hydrazides has been proposed. In addition, 3-(phenylthio)-1-indole was obtained on a multi-gram scale.
实现了一种以磺酰肼为硫源,在水相中通过碘伏催化吲哚的亚磺酰化反应来合成3-亚磺酰基吲哚。值得注意的是,碘伏作为催化剂和溶剂价格低廉、可商购且对环境无害。该方法操作也简便。此外,该合成策略的底物范围广泛,对各种官能团具有出色的耐受性。已提出了一种关于碘伏介导的吲哚与磺酰肼的3-亚磺酰化反应的合理机理。此外,还以多克规模获得了3-(苯硫基)-1-吲哚。