1‐n‐Butyl‐3‐Methylimmidazolium Tetrafluoroborate–Promoted Green Synthesis of 5‐Arylidene Barbituric Acids and Thiobarbituric Acid Derivatives
- 1 November 2005
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 35 (21), 2759-2764
- https://doi.org/10.1080/00397910500288254
Abstract
The room temperature ionic liquid 1‐n‐butyl‐3‐methylimmidazolium tetrafluoroborate ([bmim]BF4) was used to promote the synthesis of 5‐arylidene barbituric acids and thiobarbituric acid derivatives under the solid‐state conditions of grinding or microwave irradiation without organic solvent. The yields were 77.9–96.2%. It is shown that the proposed method is fast, efficient, and environmentally benign.Keywords
This publication has 4 references indexed in Scilit:
- Syntheses of Heterocyclic Compounds under Microwave IrradiationHETEROCYCLES, 2004
- Comparative kinetic investigations in ionic liquids using the MTO/peroxide systemJournal of Molecular Catalysis A: Chemical, 2002
- Ionic Liquid (Molten Salt) Phase Organometallic CatalysisChemical Reviews, 2002
- Microwave assisted organic reactionsTetrahedron, 1995