22dimethoxypropane

2,2-Dimethoxypropane, also known as acetone dimethyl acetal or di-methyl acetal of acetone, is an organic compound used primarily as a protecting group in carbonyl chemistry. Its molecular formula is C5H12O2, and it features an isopropylidene framework with two methoxy substituents attached to a central carbon.

The compound is typically prepared by acid-catalyzed acetalization of acetone with methanol. In practice, acetone and an excess of methanol are heated in the presence of a catalytic acid such as p-toluenesulfonic acid or sulfuric acid, with water removal to drive the equilibrium toward acetal formation. The reaction is reversible, and hydrolysis under acidic conditions regenerates acetone and methanol.

In organic synthesis, 2,2-dimethoxypropane is valued for protecting carbonyl groups. Converting aldehydes or ketones to their corresponding acetals temporarily blocks reactivity at the carbonyl, allowing other transformations to proceed. The acetal is stable under many neutral and basic conditions but can be cleaved back to the carbonyl compound and methanol under acidic hydrolysis. Deprotection is commonly performed when the protected functionality is needed again.

Properties and safety: 2,2-dimethoxypropane is a colorless liquid that is miscible with many organic solvents and relatively less miscible with water. It is flammable and should be handled with appropriate safety precautions. Hydrolysis or protective-use procedures should be conducted in well-ventilated areas, using suitable containment and personal protective equipment.