Related Experiment Video
Updated: Jun 14, 2025

Light-driven Enzymatic Decarboxylation
Published on: May 22, 2016
Direct Hydrodecarboxylation of Carboxylic Acids via N-Hydroxyphthalimide-Mediated Hydrogen Atom Transfer
Si-Yu Gao1, Yi-Yang Tang1, Lan Yang1
1College of Sciences, Tianjin University of Science and Technology, Tianjin 300457, P. R. China.
Abstract:
The hydrodecarboxylation of carboxylic acids is a fundamental functional group transformation in chemistry. However, current methods rely on acid preactivation, expensive photocatalysts, or transition-metal catalysts. Herein, we describe an unprecedented transition-metal- and photocatalyst-free chemoselective hydrodecarboxylation of carboxylic acids via N-hydroxyphthalimide-mediated hydrogen atom transfer. This mild method exhibits broad functional group tolerance and enables the conversion of primary, secondary, and tertiary carboxylic acids to alkanes. The versatility of this method is demonstrated through the late-stage functionalization of complex natural products and pharmaceuticals.
Related Concept Videos
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Preparation of Carboxylic Acids: Hydrolysis of Nitriles
α-Halogenation of Carboxylic Acid Derivatives: Overview
Carboxylic Acids to Primary Alcohols: Hydride Reduction
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Nitriles to Carboxylic Acids: Hydrolysis

