1‐Butyl‐3‐methylimidazolium Tetrafluoroborate ([Bmim]BF4) Ionic Liquid: A Novel and Recyclable Reaction Medium for the Synthesis of vic‐Diamines
J. S. Yadav, B. V. Subba Reddy, K. Premalatha
Abstract
J. S. Yadav, B. V. Subba Reddy, K. Premalatha
Abstract
Abstract Aziridines undergo ring opening smoothly with various arylamines in 1‐butyl‐3‐methylimidazolium tetrafluoroborate ([bmim]BF4) or 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([bmim]PF6) ionic liquids under mild and neutral conditions to afford the corresponding vicinal‐diamines in excellent yields with high regioselectivity. The recovered activated ionic liquids are recycled for four to five runs with no loss of activity.
OpenAlex reports 43 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Abstract Aziridines undergo ring opening smoothly with various arylamines in 1‐butyl‐3‐methylimidazolium tetrafluoroborate ([bmim]BF4) or 1‐butyl‐3‐methylimidazolium hexafluorophosphate ([bmim]PF6) ionic liquids under mild and neutral conditions to afford the corresponding vicinal‐diamines in excellent yields with high regioselectivity. The recovered activated ionic liquids are recycled for four to five runs with no loss of activity.
Key concepts: Ionic liquid, Tetrafluoroborate, Hexafluorophosphate, Chemistry, Regioselectivity, Vicinal, Medicinal chemistry, Organic chemistry