Abstract
The reactions of propargylic alcohols, aliphatic primary amines, and CO2 were conducted in CuCl/ [BMIm]BF4 system to produce the corresponding 5-methylene-1,3-oxazolidin-2-ones under relatively mild conditions. The products could be conveniently isolated by means of liquid-liquid extraction. The solvent ionic liquid as well as CuCl catalyst can be recovered and reused three times without appreciable loss of activity. By this green approach, several new 5-ethylene-1,3-oxazolidin-2-ones were prepared in excellent yields and purity and were well-characterized.
| Original language | English |
|---|---|
| Pages (from-to) | 7376-7380 |
| Number of pages | 5 |
| Journal | Journal of Organic Chemistry |
| Volume | 70 |
| Issue number | 18 |
| DOIs | |
| State | Published - 2 Sep 2005 |
| Externally published | Yes |