Related Experiment Video
Updated: Sep 19, 2026

Facile Preparation of 4-Substituted Quinazoline Derivatives
Published on: February 15, 2016
Preparation, characterization, and catalytic performance of a 2,3-dihydroxybenzoic acid-based deep eutectic solvent
Hadis Goudarzi1, Davood Habibi1, Abdolhamid Alizadeh2
1Department of Organic Chemistry, Faculty of Chemistry and Petroleum Chemistry, Bu-Ali Sina University Hamedan 6517838683 Iran davood.habibi@gmail.com dhabibi@basu.ac.ir +98 81 31408025 +98 81 31406070.
Abstract:
An ethyltriphenylphosphonium bromide/2,3-dihydroxybenzoic acid deep eutectic solvent (ETPPBr/2,3-DHBA-DES, 1 : 2 molar ratio) was prepared and characterized by eutectic phase behavior analysis, FT-IR spectroscopy, 1H NMR spectroscopy, TGA/DTA, and density measurements, confirming the formation of a eutectic system. The DES was then employed as a recyclable catalyst for the one-pot three-component synthesis of 6H-benzo[h]chromeno[4,3-b]quinolin-6-ones via the condensation of 4-hydroxycoumarin, 1-naphthylamine, and aryl or heteroaryl aldehydes under solvent-free conditions. Under the optimized reaction conditions (0.50 mmol catalyst, 80 °C), ten target derivatives were obtained in 60.8-85.0% isolated yields within 45-90 min. The catalyst was readily recovered by aqueous extraction and reused for four consecutive cycles, affording product yields from 85% in the first run to 72% in the fourth. FT-IR analysis of the recovered catalyst indicated that its characteristic structural features were largely preserved after recycling. These results demonstrate that the ETPPBr/2,3-DHBA-DES is an effective and recyclable catalyst for the solvent-free synthesis of 6H-benzo[h]chromeno [4,3-b]quinolin-6-ones.
Related Concept Videos
Hydrolysis of Chlorobenzene to Phenol: Dow Process
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Nucleophilic Aromatic Substitution: Elimination–Addition
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Electrophilic Aromatic Substitution: Sulfonation of Benzene
