The Journal of Organic Chemistry

New synthesis of isoxazoles and isothiazoles. A convenient synthesis of thioenaminones from enaminones

Y Lin, SA Lang Jr

Index: Lin, Yang-i; Lang, Stanley, A. Journal of Organic Chemistry, 1980 , vol. 45, # 24 p. 4857 - 4860

Full Text: HTML

Citation Number: 62

Abstract

The reaction of l-aryl-3-(dimethylamino)-2-propen-l-ones (enaminones) and l-aryl-3- (dimethylamino)-2-propene-1-thiones (thioenaminones) with hydroxylamine-0-sulfonic acid gave, respectively, isoxmoles in 76-84% yields and isothiazoles in 60-65% yields. The reaction of enaminones with phosphorus oxychloride, followed by treatment with sodium perchlorate and reaction with sodium sulfide, gave thioenaminones in 4&73% yields.

 Related Synthetic Route

~65%

Learn More

~%

Learn More

~%

Learn More

~%

Learn More

~76%

Learn More

~83%

Learn More

~91%

Learn More

~60%

Learn More

~%

Learn More

~%

Learn More

~84%

Learn More

~70%

Learn More

~%

Learn More

~%

Learn More

~60%

Learn More

~%

Learn More

~%

Learn More

~%

Learn More

~88%

Learn More

~62%

Learn More

~%

Learn More

~%

Learn More

~%

Learn More

~70%

Learn More

~%

Learn More

~%

Learn More

~63%

Learn More

~%

Learn More

~%

Learn More

~%

Learn More