Iron(II)-triflate catalyzed synthesis of 3,4-dihydropyrimidin-2(1H)-ones via the Biginelli reaction

Major

Biochemistry

Submission Type

Poster

Area of Study or Work

Chemistry

Faculty Advisor

Ram S. Mohan

Location

CNS Atrium

Start Date

4-11-2026 11:15 AM

End Date

4-11-2026 12:30 PM

Abstract

Dihydropyrimidinone scaffolds have attracted attention due to their biological activities and ease of construction. The most common pathway to these molecules is the Biginelli reaction, a multicomponent reaction involving an aldehyde, urea and a β-keto ester. This one-pot reaction is usually catalyzed by a Brønsted or Lewis acid. Many catalysts have been reported for the Biginelli reaction, such as FeCl3 , TaBr5 , and TiCp2Cl2. Some of these catalysts are toxic, not environmentally friendly, and hard to handle. Iron(III) and iron(II) salts are effective Lewis acid catalysts in various organic transformations, but iron(II) salts are less explored. Iron(II) triflate is relatively inexpensive, easy to handle, and nontoxic, making it attractive from a green chemistry perspective. We report the use of iron(II) triflate as an efficient catalyst for the Biginelli reaction.

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Apr 11th, 11:15 AM Apr 11th, 12:30 PM

Iron(II)-triflate catalyzed synthesis of 3,4-dihydropyrimidin-2(1H)-ones via the Biginelli reaction

CNS Atrium

Dihydropyrimidinone scaffolds have attracted attention due to their biological activities and ease of construction. The most common pathway to these molecules is the Biginelli reaction, a multicomponent reaction involving an aldehyde, urea and a β-keto ester. This one-pot reaction is usually catalyzed by a Brønsted or Lewis acid. Many catalysts have been reported for the Biginelli reaction, such as FeCl3 , TaBr5 , and TiCp2Cl2. Some of these catalysts are toxic, not environmentally friendly, and hard to handle. Iron(III) and iron(II) salts are effective Lewis acid catalysts in various organic transformations, but iron(II) salts are less explored. Iron(II) triflate is relatively inexpensive, easy to handle, and nontoxic, making it attractive from a green chemistry perspective. We report the use of iron(II) triflate as an efficient catalyst for the Biginelli reaction.