Related Experiment Video
Updated: Jul 4, 2025

Synthesis of Esters Via a Greener Steglich Esterification in Acetonitrile
Published on: October 30, 2018
Straightforward access to α-carbonyloxy esters and β-keto thioethers from aryldiazoacetates
Naveen Kumar1, Ajay Kant Gola1, Satyendra Kumar Pandey1
1Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi 221 005, India. skpandey.chem@bhu.ac.in.
Abstract:
A metal- and additive-free approach has been described for synthesizing α-carbonyloxy esters and β-keto thioethers from readily available aryldiazoacetates with carboxylic acids and thiol derivatives, respectively. α-Carbonyloxy esters and β-keto thioether derivatives were synthesized in good to high yields from aryldiazoacetates, carboxylic acids, and thiol derivatives decorated with various functional groups. Finally, the potential of the new approach is demonstrated through its application in gram-scale reactions and the synthesis of a few bioactive molecules.
More Related Videos
06:46Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
06:31Highly Stereoselective Synthesis of 1,6-Ketoesters Mediated by Ionic Liquids: A Three-component Reaction Enabling Rapid Access to a New Class of Low Molecular Weight Gelators
Published on: November 27, 2015
Related Concept Videos
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview
Aldol Condensation with β-Diesters: Knoevenagel Condensation
Esters to β-Ketoesters: Claisen Condensation Mechanism
Carboxylic Acids to Methylesters: Alkylation using Diazomethane