| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5409867 | Journal of Molecular Liquids | 2016 | 5 Pages |
â¢Synthesis of benzo[d]imidazoles using [DABCO] diacetateâ¢Green protocol in short reaction time with excellent yieldsâ¢This method's benefits are easy purification and solvent-free conditions.
A general synthetic route to benzo[d]imidazoles has been developed using 1,4-diazabicyclo [2.2.2] octanium diacetate as a new bis ionic liquid under thermal and solvent free condition. The union of two fragments including one equivalent of various aldehydes and one equivalent of 1,2-phenylenediamine was accomplished by an efficient and convenient protocol enabling the synthesis of benzo[d]imidazoles in excellent yields. The major advantages of the present method are: less reaction times, high yields, and easy purification of the products, solvent-free conditions, environmental friendliness, and convenient operation.
![First Page Preview: 1,4-Diazabicyclo [2.2.2] octanium diacetate: As an effective, new and reusable catalyst for the synthesis of benzo[d]imidazole 1,4-Diazabicyclo [2.2.2] octanium diacetate: As an effective, new and reusable catalyst for the synthesis of benzo[d]imidazole](/preview/png/5409867.png)