4.3 Article

Simple and efficient procedure for the one-pot synthesis of beta-acetamido-beta-aryl-propiophenones by molecular iodine-catalyzed tandem reaction

Journal

SYNTHETIC COMMUNICATIONS
Volume 37, Issue 7-9, Pages 1551-1556

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397910701234982

Keywords

beta-acetamido-beta-aryl-propiophenones; acetonitrile; acetyl chloride; arylaldehydes; arylmethyl ketones; iodine

Ask authors/readers for more resources

Molecular iodine efficiently catalyzes the four-component tandem reaction of araldehydes, arylmethyl ketones, acetyl chloride, and acetonitrile to afford the corresponding beta-acetamido-beta-aryl-propiophenones. The new protocol gives high yields of the products, and the reactions go to completion within 10-15 min on a hot plate at 80-85 degrees C.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available