An Efficient Green Protocol for Synthesis Of 2,3-Dihydroquinazolin-4(1H)-Ones Using Mandelic Acid Under Solvent-Free Conditions

Green and convenient synthesis of 2,3-dihydroquinazolin- 4(1H)- one derivatives (DHQ) from condensation of 2-aminobenzamide and various aromatic aldehydes using Mandelic acid under Solvent‐Free Conditions. The present method has some important advantages such as mild reaction conditions, use of naturally occurring commercially available low cost organocatalyst, short reaction times and high yields with the green protocol by avoiding toxic catalysts and solvents, column chromatography-free purification procedure are some of the major advantages of this developed protocol.

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Publication Details

Journal
International Journal of Scientific Research in Science Engineering and Technology
Published
2024-12-11
DOI
https://doi.org/10.32628/ijsrset24116183
Primary Topic
Quinazolinone synthesis and applications
Type
article
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article

An Efficient Green Protocol for Synthesis Of 2,3-Dihydroquinazolin-4(1H)-Ones Using Mandelic Acid Under Solvent-Free Conditions

Jeevanand Deshmukh, Uddhav N. Chaudhar, Shivanand G. Sonkamble, A. M. Patil
International Journal of Scientific Research in Science Engineering and Technology
Quinazolinone synthesis and applications
article

An Efficient Green Protocol for Synthesis Of 2,3-Dihydroquinazolin-4(1H)-Ones Using Mandelic Acid Under Solvent-Free Conditions

Jeevanand Deshmukh, Uddhav N. Chaudhar, Shivanand G. Sonkamble, A. M. Patil
article en

Abstract

Green and convenient synthesis of 2,3-dihydroquinazolin- 4(1H)- one derivatives (DHQ) from condensation of 2-aminobenzamide and various aromatic aldehydes using Mandelic acid under Solvent‐Free Conditions. The present method has some important advantages such as mild reaction conditions, use of naturally occurring commercially available low cost organocatalyst, short reaction times and high yields with the green protocol by avoiding toxic catalysts and solvents, column chromatography-free purification procedure are some of the major advantages of this developed protocol.

International Journal of Scientific Research in Science Engineering and TechnologyVol. 11(6)
G.S. Science, Arts And Commerce College (IN)
Openalex Percentile: Top 83%
Quinazolinone synthesis and applications
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