Ethyl acetate is one of the simplest carboxylate esters. (Former Molecule of the Week methyl formate is the simplest.) The colorless liquid has a sweet, fruity odor that most people find pleasant.
As you might expect, ethyl acetate was first synthesized from ethanol and acetic acid. The reaction was the classic acid-catalyzed Fischer esterification, which dates back to 1895. This is still the most widely used commercial synthesis. An alternative method is the Tishchenko reaction in which acetaldehyde disproportionates in the presence of base to the alcohol and the acid that then esterify in situ.
Ethyl acetate is a widely used solvent, especially for paints, varnishes, lacquers, cleaning mixtures, and perfumes. Like last week’s MOTW, dichloromethane, it is used as a solvent for decaffeinating coffee beans. In the lab, ethyl acetate is a common solvent for column and thin-layer chromatography.