Lithium Chloride-Promoted Brønsted Acid-Catalyzed Friedel-Crafts Alkylation Reaction of Indoles with Aldehydes and Ketones “on Water”
  • Yang, Jun
  • Zhang, Jianyu
  • Li, Tianxing
  • Liu, Yunting
  • Jin, Hui
  • ... Ryu, Do Hyun
  • 외 1명
Citations

WEB OF SCIENCE

1
Citations

SCOPUS

3

초록

The Friedel-Crafts reaction between indoles and ketones poses a significant challenge. In this study, we developed an efficient and environmentally friendly approach for the synthesis of bis(indolyl)methanes bearing all-carbon quaternary and tertiary centers at room temperature under “on water” conditions. Notably, the utilization of saturated lithium chloride as a solvent greatly enhances the Brønsted acid-catalyzed double additions of indoles to ketones and aldehydes by promoting hydrophobic interactions. Additionally, LiCl acts as a Lewis acid catalyst for carbonyl activation and facilitates dehydration. This methodology demonstrates compatibility with various ketone substrates such as alkyl alkyl ketones and aryl alkyl ketones, along with aldehyde substrates. Furthermore, gram-scale productions were successful, and the LiCl solutions demonstrate reusability. © 2025 Wiley-VCH GmbH.

키워드

Bis(indoly)methaneBrønsted acidLewis acidLithium chlorideon WaterDIELS-ALDER REACTIONONE-POT SYNTHESISORGANIC-REACTIONSLEWISBIS(INDOLYL)METHANESEFFICIENTAMPLIFICATIONACCELERATIONACTIVATIONBEARING
제목
Lithium Chloride-Promoted Brønsted Acid-Catalyzed Friedel-Crafts Alkylation Reaction of Indoles with Aldehydes and Ketones “on Water”
저자
Yang, JunZhang, JianyuLi, TianxingLiu, YuntingJin, HuiRyu, Do HyunZhang, Lixin
DOI
10.1002/adsc.202401542
발행일
2025-05
유형
Article; Early Access
저널명
Journal für Praktische Chemie
367
9