acetalsketals

Acetals and ketals are classes of organic functional groups formed when carbonyl compounds react with alcohols. An acetal is the product derived from an aldehyde, while a ketal comes from a ketone. In both cases the carbonyl oxygen is replaced by two alkoxy groups (OR). For acetals, the acetal carbon typically bears one hydrogen and two OR groups; for ketals, the acetal carbon bears two carbon substituents and two OR groups.

Formation and hydrolysis occur under acid catalysis and with removal of water. Aldehydes react with two equivalents of an alcohol to give an acetal, and ketones react similarly to give a ketal. The process is reversible: exposure to aqueous acid hydrolyzes acetals and ketals back to the original carbonyl compound plus alcohols. This equilibrium can be driven toward acetal or ketal formation by removing water or using dehydrating conditions.

Acetals and ketals are widely used as protective groups for carbonyl compounds in organic synthesis. They tend to be stable under basic and many neutral conditions, but can be selectively cleaved to regenerate the carbonyl under acidic aqueous workups. Cyclic acetals and ketals, formed with diols such as ethylene glycol or propylene glycol, are particularly common and give five- or six-membered rings (for example 1,3-dioxolanes and 1,3-dioxanes) that serve as robust protecting groups for aldehydes and ketones.

Examples include acetaldehyde dimethyl acetal (an acetal derived from acetaldehyde) and various cyclic acetals/ketals used to shield carbonyl functionality during multistep syntheses. The choice between acetal or ketal protection depends on whether the starting carbonyl is an aldehyde or a ketone, as well as the desired stability under subsequent reaction conditions.