acetalisation

Acetalisation is a chemical reaction in which an aldehyde or ketone reacts with a diol to form an acetal. The reaction is typically catalysed by a Lewis or Brønsted acid and proceeds via a protonation step that activates the carbonyl group. The diol then nucleophilically attacks the activated carbonyl carbon, leading to the formation of a hemiacetal intermediate. Subsequent proton transfers and substitution of a water molecule result in the final acetal product. The general scheme can be represented as R2C=O + HO–R'–R"–OH → R2C(OR')–OR" + H2O. Because the reaction removes water, it is often driven to completion by the use of a dehydrating agent such as anhydrous reagents or by distillation of water in excess. Reversible acetalisation, called acetal exchange, allows the conversion of the acetal to the original carbonyl compound by treatment with a protic acid, making the reaction reversible under appropriate conditions.

Acetals are valuable as protecting groups for carbonyl functionalities in organic synthesis, as the acetal protects the underlying aldehyde or ketone from oxidation or other side reactions. In industrial chemistry, acetalisation is employed in the synthesis of diols like 1,3-butanediol and in the production of polymer precursors such as polyacetals. The reaction's mild conditions and high selectivity make it attractive for fine chemical manufacturing. Safety considerations include the handling of strong acids and potential exothermicity when water is evolved rapidly. Appropriate ventilation and temperature control mitigate these hazards.