Diethyl(phenylacetyl)malonate, also recognized as CAS registry number 20320-59-6, is a synthesized compound. It is a viscous colorless oil with a characteristic odor. This chemical reagent is widely used in research laboratories for its ability to react with other compounds.
The structure of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonate diester. This molecular design allows it to participate in various reactions.
Chemical Synthesis of Diethyl(phenylacetyl)malonate
The synthesis of diethyl(phenylacetyl)malonate is a fundamental reaction in organic chemistry. This compound serves as a valuable building block for the production of various complex molecules, particularly in the field of pharmaceuticals and agrochemicals. The synthesis typically involves a two-step process. In the initial step, phenylacetic acid reacts with ethanol in the presence of an acidic reagent, such as sulfuric acid. This reaction yields phenyl acetate ester, which is then treated to malonic ester. The final product, diethyl(phenylacetyl)malonate, is obtained after a series of chemical transformations involving combination.
- The reaction conditions play a crucial role in determining the yield and purity of the final product.
- Various purification techniques, such as recrystallization or column chromatography, can be employed to isolate the desired compound.
- Safety precautions must be taken during the synthesis process, as some reagents involved may be hazardous.
Description of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a molecule with the chemical formula C15H18O4. This ester can be prepared through several methods, often involving the process of phenylacetic acid with diethyl malonate. It exhibits unique physical properties, such as a color that ranges from colorless to light yellow and a temperature of around 270°C.
- Significant structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found applications in various organic processes.
- More research continues to explore its potential in the development of novel compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate possesses a distinct set of physicochemical properties that contribute its reactivity and applications. Its structural formula, C16H18O4, reflects the presence of an array of ethyl ester groups and the phenylacetyl moiety. The Product Categories: 20320-59-6 material's molar mass is around 274.31 g/mol, indicating its considerable weight. At room temperature, diethyl(phenylacetyl)malonate exists as a liquid state with a distinctive odor. Its miscibility in common organic solvents is to be high. The compound's melting point varies depending on purity and factors. Its boiling point, on the other hand, falls within a determined range. The presence of functional groups within its structure impacts its intermolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate plays a crucial part in organic reactions due to its versatile arrangement. This molecule can be readily modified through various organic processes to yield a wide range of valuable products. For illustration, diethyl(phenylacetyl)malonate can be used in the preparation of pharmaceuticals, agrochemicals, and various chemical products.
One notable use is its role in the synthesis of alcohols with an ester group, which are often employed as intermediates in the construction of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the synthesis of heterocyclic compounds, which are essential components of many natural products and pharmaceuticals.
Diethyl(phenylacetyl)malonate (C15H18O5): A Versatile Building Block
Diethyl(phenylacetyl)malonate (C15H18O5), a compound possessing a distinctive structure, has emerged as a powerful building block in organic synthesis. Its remarkable reactivity profile allows for the synthesis of elaborate molecular architectures across various chemical domains. This flexible molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.