Related Experiment Video
Updated: Apr 30, 2026

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
Direct Synthesis of Amides from Nitro Compounds and Alcohols via Borrowing Hydrogenation∇
Padmavathy V K Nair1, Gourishankar B Swami1, Boopathy Gnanaprakasam1
1Department of Chemistry, Indian Institute of Science Education and Research, Pune-411008, India.
Abstract:
Herein, we report a RuH2(CO)(PPh3)3 catalyzed direct amidation of alcohols using readily available nitro compounds via a catalytic borrowing hydrogen method. This reaction proceeded via cascade reactions, including oxidation of alcohol, reduction of nitro group and formation of amides under one-pot condition. This protocol provides a single catalytic system for many reactions, a step economic advantage over the available techniques, tolerates various functionalities, and was demonstrated with broad substrate scope (47 examples).
Related Concept Videos
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Acid Halides to Esters: Alcoholysis
Preparation of 1° Amines: Gabriel Synthesis
Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
Production of Organic Acids

