The synthesis of iodoform was first described by
Georges-Simon Serullas in 1822, by reactions of iodine vapour with steam over red-hot coals, and also by reaction of potassium with ethanolic iodine in the presence of water; and at much the same time independently by
John Thomas Cooper. It is synthesized in the
haloform reaction by the reaction of iodine and sodium hydroxide with any one of these four kinds of organic compounds: a methyl
ketone (),
acetaldehyde (),
ethanol (), and certain secondary
alcohols (, where R is an alkyl or aryl group). : The reaction of iodine and base with
methyl ketones is so reliable that the
iodoform test (the appearance of a yellow precipitate) is used to probe the presence of a methyl ketone. This is also the case when testing for specific
secondary alcohols containing at least one
methyl group in
alpha-position. Some reagents (e.g.
hydrogen iodide) convert iodoform to
diiodomethane. Conversion to
carbon dioxide is also possible. Iodoform reacts with aqueous
silver nitrate to produce
carbon monoxide. When treated with powdered elemental silver the iodoform is reduced, producing
acetylene. Upon heating iodoform decomposes to produce diatomic iodine, hydrogen iodide gas, and carbon.
Natural occurrence The
angel's bonnet mushroom contains iodoform, and shows its characteristic odor. ==Applications==