Dakin–West reaction

From WikiMD's Wellness Encyclopedia

Dakin–West reaction is an organic chemistry reaction that involves the transformation of carboxylic acids into their corresponding acyl ketones through the reaction with acetic anhydride in the presence of a base. This reaction was first reported by Henry Drysdale Dakin and Randolph West in 1928. The Dakin–West reaction is particularly useful for synthesizing β-ketoesters and amides, making it a valuable tool in the synthesis of complex organic molecules.

Mechanism[edit | edit source]

The mechanism of the Dakin–West reaction begins with the deprotonation of the carboxylic acid by a base, typically pyridine, to form a carboxylate anion. This anion then reacts with acetic anhydride, leading to the formation of a mixed anhydride intermediate. Subsequent intramolecular acylation and elimination steps yield the β-ketoester or amide product. The reaction is characterized by its ability to introduce an acyl group at the α-position of a carboxylic acid in a single step.

Applications[edit | edit source]

The Dakin–West reaction has found applications in various fields of organic synthesis. It is particularly useful in the synthesis of complex molecules such as natural products, pharmaceuticals, and agrochemicals. The ability to efficiently synthesize β-ketoesters and amides, which are important intermediates in organic synthesis, makes the Dakin–West reaction a valuable tool for chemists.

Limitations[edit | edit source]

Despite its utility, the Dakin–West reaction has some limitations. The reaction conditions can be harsh, and sensitive functional groups may not be compatible with the reaction conditions. Additionally, the reaction typically requires a strong base, which can lead to side reactions or decomposition of the starting materials.

Variants[edit | edit source]

Several variants of the Dakin–West reaction have been developed to overcome its limitations and expand its applicability. These include modifications of the reaction conditions, the use of different bases, and the application of the reaction to different types of starting materials. These variants have broadened the scope of the Dakin–West reaction, making it a more versatile tool in organic synthesis.

See also[edit | edit source]

References[edit | edit source]


WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD