2014Fain kemikaruRequires access

One-Pot Synthesis of 4-Phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydropyrimidin-2( H)-ketone Catalyzed by H_4SiW_(12)O_(40)/SiO_2

Gong Wen-pen

Open publisher page 0 citations

Abstract

H 4 SiW 12 O 40 / SiO 2 exhibited excellent catalytic performance for the synthesis of 4-phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydro-pyrimidin-2( H)-ketone via one-pot Biginelli reaction from benzaldehyde,ethyl acetoacetate,and urea with anhydrous ethanol as solvent. The effects of the various reaction parameters on the yield of the product were investigated and the optimum conditions were determined as follows: fixed benzaldehyde consumption was 0. 04 mol,n( benzaldehyde) ∶ n( ethylacetoacetate) ∶n( urea) =1∶1. 5∶1. 5,the quantity of catalyst was 2. 0% of the feed stock,reaction temperature was 90 ℃,and reaction time was 1. 0 h. Under such conditions,the yield of the product was up to 71. 7%. The 3,4-dihydropyrimidin-2( H)-ketone was characterized by means of melting point measurements,IR,1HNMR and MS spectroscopy.

About this research paper

What this paper is about

H 4 SiW 12 O 40 / SiO 2 exhibited excellent catalytic performance for the synthesis of 4-phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydro-pyrimidin-2( H)-ketone via one-pot Biginelli reaction from benzaldehyde,ethyl acetoacetate,and urea with anhydrous ethanol as solvent. The effects of the various reaction parameters on the yield of the product were investigated and the optimum conditions were determined as follows: fixed benzaldehyde consumption was 0. 04 mol,n( benzaldehyde) ∶ n( ethylacetoacetate) ∶n( urea) =1∶1. 5∶1. 5,the quantity of catalyst was 2. 0% of the feed stock,reaction temperature was 90 ℃,and reaction time was 1. 0 h. Under such conditions,the yield of the product was up to 71. 7%. The 3,4-dihydropyrimidin-2( H)-ketone was characterized by means of melting point measurements,IR,1HNMR and MS spectroscopy.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

H 4 SiW 12 O 40 / SiO 2 exhibited excellent catalytic performance for the synthesis of 4-phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydro-pyrimidin-2( H)-ketone via one-pot Biginelli reaction from benzaldehyde,ethyl acetoacetate,and urea with anhydrous ethanol as solvent. The effects of the various reaction parameters on the yield of the product were investigated and the optimum conditions were determined as follows: fixed benzaldehyde consumption was 0. 04 mol,n( benzaldehyde) ∶ n( ethylacetoacetate) ∶n( urea) =1∶1. 5∶1. 5,the quantity of catalyst was 2. 0% of the feed stock,reaction temperature was 90 ℃,and reaction time was 1. 0 h. Under such conditions,the yield of the product was up to 71. 7%. The 3,4-dihydropyrimidin-2( H)-ketone was characterized by means of melting point measurements,IR,1HNMR and MS spectroscopy.

Key concepts: Benzaldehyde, Catalysis, Chemistry, Yield (engineering), Ethyl acetoacetate, Urea, Anhydrous, Ketone

Related papers

Back to paper searchBrowse research topicsOriginal source
One-Pot Synthesis of 4-Phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydropyrimidin-2( H)-ketone Catalyzed by H_4SiW_(12)O_(40)/SiO_2 — Research Paper | ScholarLens