Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthetic organic molecule. It is a white crystalline solid with a distinctive aroma. This organic compound is widely used in research get more info laboratories for its ability to serve as a precursor.
The structure of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonic ester derivative. This molecular design allows it to undergo transformations.
Chemical Synthesis of Diethyl(phenylacetyl)malonate
The preparation of diethyl(phenylacetyl)malonate is a fundamental reaction in organic chemistry. This compound serves as a valuable building block for the preparation of various complex molecules, particularly in the field of pharmaceuticals and agrochemicals. The synthesis typically involves a two-step process. In the first step, phenylacetic acid reacts with ethanol in the presence of an acidic promoter, such as sulfuric acid. This reaction yields phenyl acetate ester, which is then subjected 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.
Analysis of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a molecule with the chemical formula C15H18O4. This ester can be synthesized through several methods, often involving the process of phenylacetic acid with diethyl malonate. It exhibits characteristic physical attributes, such as a color that ranges from colorless to light yellow and a vaporization point 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 chemical reactions.
- Further research continues to explore its potential in the synthesis of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that influence its reactivity and applications. Its molecular formula, C16H18O4, reflects the presence of multiple ethyl ester groups and the phenylacetyl moiety. The compound's molar mass is roughly 274.31 g/mol, indicating its considerable weight. At room temperature, diethyl(phenylacetyl)malonate exists as a solid state with a specific odor. Its solubility in common organic solvents proves to be limited. The compound's melting point fluctuates depending on purity and influences. Its boiling point, on the other hand, resides within a determined range. The presence of polar groups within its structure impacts its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial role in organic synthesis due to its versatile composition. This compound can be readily transformed through various synthetic transformations to yield a wide collection of valuable products. For illustration, diethyl(phenylacetyl)malonate can be employed in the synthesis of medicines, agrochemicals, and diverse organic substances.
One notable application is its role in the creation of beta-hydroxy esters, which are frequently employed as precursors in the assembly of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the creation of ring-containing compounds, which are essential elements of many natural products and pharmaceuticals.
Diethyl(phenylacetyl)malonate (C15H18O5): A Versatile Building Block
Diethyl(phenylacetyl)malonate (C15H18O5), a compound containing a distinctive structure, has emerged as a potent building block in organic synthesis. Its remarkable reactivity profile allows for the synthesis of diverse molecular architectures across diverse chemical domains. This robust molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.