Grignard reaction


The Grignard reaction is an organometallic chemical reaction in which alkyl, allyl, vinyl, or aryl-magnesium halides add to a carbonyl group in an aldehyde or ketone. This reaction is important for the formation of carbon–carbon bonds. The reaction of an organic halide with magnesium is not a Grignard reaction, but provides a Grignard reagent.
Grignard reactions and reagents were discovered by and are named after the French chemist François Auguste Victor Grignard, who published it in 1900 and was awarded the 1912 Nobel Prize in Chemistry for this work.

Reaction mechanism

The carbon attached to magnesium functions as a nucleophile, attacking the electrophilic carbon atom that is present within the polar bond of a carbonyl group. The addition of the Grignard reagent to the carbonyl typically proceeds through a six-membered ring transition state.