<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(31)</volume><submitter>Ponpao N</submitter><pubmed_abstract>A green, convenient, and metal-free methodology for synthesizing primary aniline-based indolylmethanes has been developed through a sequential one-pot, three-component aza-Friedel-Crafts reaction. This approach employs a wide range of commercially available aldehydes, primary anilines, and indoles, catalyzed by a Brønsted acidic ionic liquid in an aqueous medium. A variety of desirable products were obtained in high yields (up to 98%). The process was successfully demonstrated on a gram scale, confirming its scalability and reproducibility while maintaining high yields. Additionally, the catalyst exhibited remarkable recyclability, retaining high catalytic efficiency over three cycles without a significant loss of activity.</pubmed_abstract><journal>ACS omega</journal><pagination>34951-34963</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12355243</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Green Synthesis of Primary Aniline-Based Indolylmethanes via One-Pot Aza-Friedel-Crafts Reaction Catalyzed by Bronsted Acidic Ionic Liquid in Aqueous Media.</pubmed_title><pmcid>PMC12355243</pmcid><pubmed_authors>Ponpao N</pubmed_authors><pubmed_authors>Sirion U</pubmed_authors><pubmed_authors>Suksai C</pubmed_authors><pubmed_authors>Masnguluem P</pubmed_authors><pubmed_authors>Jaratjaroonphong J</pubmed_authors><pubmed_authors>Trakulsujaritchok T</pubmed_authors><pubmed_authors>Senapak W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Green Synthesis of Primary Aniline-Based Indolylmethanes via One-Pot Aza-Friedel-Crafts Reaction Catalyzed by Bronsted Acidic Ionic Liquid in Aqueous Media.</name><description>A green, convenient, and metal-free methodology for synthesizing primary aniline-based indolylmethanes has been developed through a sequential one-pot, three-component aza-Friedel-Crafts reaction. This approach employs a wide range of commercially available aldehydes, primary anilines, and indoles, catalyzed by a Brønsted acidic ionic liquid in an aqueous medium. A variety of desirable products were obtained in high yields (up to 98%). The process was successfully demonstrated on a gram scale, confirming its scalability and reproducibility while maintaining high yields. Additionally, the catalyst exhibited remarkable recyclability, retaining high catalytic efficiency over three cycles without a significant loss of activity.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-10T04:15:02.288Z</modification><creation>2026-04-08T01:29:36.678Z</creation></dates><accession>S-EPMC12355243</accession><cross_references><pubmed>40821540</pubmed><doi>10.1021/acsomega.5c04294</doi></cross_references></HashMap>