期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 70, 期 18, 页码 7376-7380出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo050802i
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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-methylene-1,3-oxazolidin-2-ones were prepared in excellent yields and purity and were well-characterized.
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