The
Gattermann-Koch reaction, named for the German chemists
Ludwig Gattermann and
Julius Arnold Koch, in
organic chemistry refers to a
Friedel-Crafts acylation reaction in which
carbon monoxide and hydrochloric acid are used
in-situ with
Friedel-Crafts catalyst, namely AlCl
3 to produce a
benzaldehyde-derivative from a benzene-derivative in one step. Benzaldehyde and many aromatic
aldehydes are conveniently synthesized by this reaction. Presence of traces of
copper(I) chloride are also needed.
An example would be the conversion of toluene to p-tolualdehyde.
See also
References