Abstract
Cyclization of arylamides of acetylthioacetic acid withω-bromoacetophenone gives mixtures containing hydrobromides of 2-(acetylmethylene)-3, 4-diarylthiazolines and 2-(acetylmethylene)-3, 4-diarylthiazolines, and from these mixtures hitherto undescribed substituted 4-thiazoline derivatives were isolated by chromatography. 2-(Acetylmethylene)-3-aryl-4-thiazolidones were obtained for the first time by reacting arylamides with acetylthioacetic acid with monochloroacetic acid in the presence of fused sodium acetate in glacial acetic acid.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have