Oxidation of primary alcohols to carboxylic acids

Potassium permanganate (KMnO₄) is a very strong oxidant able to react with many functional groups, such as secondary alcohols, 1,2-diols, aldehydes, alkenes, oximes, sulfides and thiols. Under controlled conditions, KMnO₄ oxidizes primary alcohols to carboxylic acids very efficiently. This reaction, which was first described in detail by Fournier,[1][2] is typically carried out by adding KMnO₄ to a solution or suspension of the alcohol in an alkaline aqueous solution. The resulting mixture is stirred until the oxidation is complete. For the reaction to proceed efficiently, the alcohol must be at least partially dissolved in the aqueous solution. This can be facilitated by the addition of an organic co-solvent such as dioxane, pyridine, acetone or t-BuOH. KMnO₄ will readily react with a carbon-carbon double bond before oxidizing a primary alcohol.

Normally, these oxidations are performed under strong basic conditions, because this promotes a greater oxidation speed and selectivity. In substrates sensitive to strong base, the reaction can be carried out at a lower pH—or even under acidic conditions—at the cost of a greatly decreased reaction velocity.

Ciufolini and Swaminathan [3] oxidized a primary alcohol to carboxylic acid with KMnO₄ in aqueous NaOH during the obtention of a rare amino acid derivative needed for the preparation of antibiotics isolated from Actinomadura luzonensis, a microorganism found in a soil sample collected in Luzon island in the Philippines

KMnO₄ is decomposed in water, resulting in formation of manganese dioxide (MnO₂) and gaseous oxygen. This decomposition is catalyzed by acid, base and MnO₂. As the extent of this decomposition is difficult to estimate during the oxidation of primary alcohols, the quantity of KMnO₄ must be adjusted during the oxidation by adding it sequentially until the oxidation is complete.

The so-called Jones reagent is prepared by dissolving chromium trioxide (CrO₃) in aqueous sulfuric acid, which results in formation of a reddish solution containing chromic acid (H₂CrO₄) and oligomers thereof. Addition of Jones reagent to a solution of a primary alcohol in acetone (as first described by Jones [4][5]) results in oxidation of the alcohol to a carboxylic acid. This classical protocol, involving a direct addition, is used very often regardless of the fact that it frequently leads to the formation of substantial amounts of esters (possessing the structure R-CO-O-CH₂-R) derived from oxidative dimerization of primary alcohols. Holland and Gilman[6] proved that this side reaction can be greatly suppressed by following the inverse addition protocol whereby a solution of the primary alcohol in acetone is slowly added to Jones reagent under conditions as dilute as practical.

Jones reagent interacts with secondary alcohols resulting in oxidation to ketones.[7] Treatment of compounds, containing both primary and secondary alcohols, with Jones reagent leads to formation of ketoacids.

Problems encountered with the use of large quantities of chromium trioxide, which is toxic and dangerous for the environment, prompted the development by Zhao [8] of a catalytic procedure, involving treatment with excess of periodic acid (H₅IO₆) in presence of about 1.2 mol% of CrO₃. Zhao's procedure for the use of catalytic CrO₃ is very well-suited for reactions on a large scale.[9]

Crimmins and DeBaillie[10] employed Zhao’s oxidation of primary alcohols to acids, using catalytic CrO₃ and excess H₅IO₆, in one step of the synthesis of Bistramide A¹, an antitumor compound isolated from the marine ascidian Lissoclinum bistratum with potential for the treatment of nonsmall cell pulmonary carcinoma.

Pyridinium dichromate (PDC) is a bright-orange solid with the formulae (C₅H₅NH)₂Cr₂O₇ that is very often used for the oxidation of primary and secondary alcohols to aldehydes and ketones respectively. On the other hand, in 1979, Corey and Schmidt reported [11] that reaction of saturated primary alcohols with PDC, using dimethylformamide (Me₂NCHO, DMF) as solvent, results in oxidation to carboxylic acids rather than aldehydes. No oxidation to carboxylic acids occurs on allylic and benzylic primary alcohols. The procedure of Corey and Schmidt for the oxidation of saturated primary alcohols to carboxylic acids is run under essentially neutral conditions.

In the heyns oxidation the oxidizing reagent is a combination of oxygen and platinum.

Ruthenium tetroxide has many uses in organic chemistry as an oxidizing agent. It is an aggressive agent allowing mild reaction conditions.

As a lot of the aforementioned conditions for the oxidations of primary alcohols to acids are harsh and not compatible with common protection groups, organic chemists often use a two-step procedure for the oxidation to acids. The primary alcohol is oxidized to an aldehyde using one of the many existing procedures (e.g. IBX oxidation, Dess–Martin periodinane). The aldehyde can then be subjected to the conditions of the Pinnick oxidation using sodium chlorite.[12] This sequence is often used in natural product synthesis, Nicolaou et al. applied it in their synthesis of Platencin.[13]

• Marcos Fernández; Gabriel Tojo (2006). Oxidation of Primary Alcohols to Carboxylic Acids: A Guide to Current Common Practice (Basic Reactions in Organic Synthesis). Berlin: Springer. ISBN 0-387-35431-X.