alkoxylation

Alkoxylation is a chemical reaction in which an alkoxy group (-OR) is introduced into a molecule. The term covers a range of transformations in organic synthesis and polymer chemistry in which alcohols or alkoxides are incorporated as substituents, forming ethers or alkoxylated products.

One major branch is O-alkylation, or ether formation, where an alkoxide reacts with an alkyl halide or other alkylating agent to yield an ether. Classic examples include the Williamson ether synthesis and related methods that produce simple or branched ethers under basic conditions. Acid-catalyzed etherifications and related condensations also contribute to alkoxylation chemistry, especially when alcohols react with activated substrates.

A second major branch involves oxyalkylation, including ethoxylation and propoxylation. In industrial processes, alcohols are reacted with epoxides or with ethylene oxide and propylene oxide to form polyethers. The resulting products, such as alkyl polyethoxylates and poly(propylene oxide) derivatives, are widely used as nonionic surfactants, lubricants, solvents, and components of detergents and coatings. These processes typically employ basic catalysts (for example, alkali hydroxides) or phase-transfer catalysts, and are conducted under controlled temperatures and pressures due to the reactive oxide monomers.

Other approaches include hydroalkoxylation, in which alcohols add across double or triple bonds in the presence of metal catalysts, leading to alkoxylated products with diverse architectures.

Applications of alkoxylation span consumer products, polymers, pharmaceuticals, and specialty chemicals, reflecting the versatility of introducing alkoxy functionalities into organic frameworks. Related topics include etherification, ethoxylation, and propoxylation.