Schmidt Rearrangement

Schmidt Rearrangement: This reaction was discovered by Karl Friedrich Schmidt in 1924. Azides (RN3) are nucleophilic at their terminal nitrogen atoms and may add to suitably activated electrophiles, such as carbonyl compounds, tertiary alcohols, or alkenes to give amines, nitriles, amides, or imines. It is an acid-catalyzed reaction. For example:

Schmidt Rearrangement

Reaction mechanism:

(i) Initially, a protonation reaction takes place and a water molecule is lost forming an acylium ion.

Reaction mechanism

(ii) The acylium ion then reacts with hydrazoic acid to form protonated azido ketone. The alkyl group shifts from carbonyl carbon to the nitrogen atom by rearrangement reaction.

Schmidt Rearrangement

(iii) A protonated isocyanate ion is formed due to the addition of a water molecule. It undergoes deprotonations to give amine and carbon dioxide.

amine and carbon dioxide.

Applications of Schmidt Rearrangement:

It is used to introduce amine, nitrile, amide, or imine, functional groups.

Applications of Schmidt Rearrangement
Make sure you also check our other amazing Article on : Oppenauer Oxidation
Sharing Is Caring:

Leave a Comment