Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthetic organic molecule. It is a viscous colorless oil with a distinctive aroma. This organic compound is widely used in research laboratories for its ability to react with other compounds.
The formula of diethyl(phenylacetyl)malonate consists of a phenylacetyl moiety attached to a malonic ester derivative. This molecular design allows it to undergo transformations.
Chemical Synthesis of Diethyl(phenylacetyl)malonate
The creation of diethyl(phenylacetyl)malonate is a fundamental reaction in organic chemistry. This compound serves as a valuable building block for the synthesis 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 catalyst, such as sulfuric acid. This reaction yields phenyl acetate ester, which is then exposed 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 compound with the chemical formula C15H18O4. This product can be prepared through several methods, often involving the process of phenylacetic acid with diethyl malonate. It exhibits characteristic physical properties, such as a shade that ranges from colorless to light yellow and a vaporization point of around 270°C.
- Important structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found applications in various chemical transformations.
- Additional research continues to explore its potential in the creation of innovative compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate possesses a distinct set of physicochemical properties that contribute its reactivity and applications. Its molecular formula, C16H18O4, reflects the presence of an array of ethyl ester groups and a phenylacetyl moiety. The compound's molar mass is around 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a solid state with a specific odor. Its dissolvability in common organic solvents remains to be moderate. The EINECS: 205-854-1 compound's melting point fluctuates depending on purity and conditions. Its boiling point, on the other hand, resides within a narrow range. The presence of reactive groups within its structure impacts its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial function in organic chemistry due to its versatile arrangement. This molecule can be readily modified through various chemical processes to yield a wide collection of valuable products. For instance, diethyl(phenylacetyl)malonate can be used in the synthesis of pharmaceuticals, agrochemicals, and other chemical substances.
One notable application is its role in the production of alcohols with an ester group, which are often employed as precursors in the formation of complex compounds.
Furthermore, diethyl(phenylacetyl)malonate can be employed in the production of organic molecules with rings, which are essential elements 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 uncommon reactivity profile allows for the fabrication of elaborate molecular architectures across diverse chemical domains. This adaptable molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.