Diethyl(phenylacetyl)malonate, also recognized as CAS registry number 20320-59-6, is a synthesized compound. It is a viscous colorless oil with a distinctive aroma. This chemical reagent is widely used in various industrial applications for its ability to form intermediates.
The composition of diethyl(phenylacetyl)malonate consists of a phenyl acetyl group attached to a malonic ester derivative. This chemical arrangement 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 preparation of various complex molecules, particularly in the field of pharmaceuticals and agrochemicals. The synthesis typically involves a two-step process. In the primary 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 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 molecule with the chemical formula C15H18O4. This product can be synthesized through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits unique physical properties, such as a shade that ranges from colorless to light yellow and a vaporization point of around 270°C.
- Key structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found uses in various chemical reactions.
- Further research continues to explore its potential in the synthesis of innovative compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate exhibits a distinct set of physicochemical properties that influence its reactivity and applications. Its molecular formula, C16H18O4, reflects the presence of an array of ethyl ester groups and a phenylacetyl moiety. The material's molar mass is roughly 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate exists as a liquid state with a distinctive odor. Its miscibility in common organic solvents remains to be moderate. The compound's transition temperature varies depending on purity and influences. Its boiling point, on the other hand, falls within a narrow range. The presence of reactive groups within its structure affects its intermolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate plays a crucial role in organic chemistry due to its versatile structure. This compound can be readily altered through various synthetic EINECS: 205-854-1 transformations to yield a wide collection of valuable products. For instance, diethyl(phenylacetyl)malonate can be employed in the preparation of medicines, pesticides, and various chemical products.
One notable utilization is its role in the production of beta-hydroxy esters, which are often employed as building blocks in the formation of complex structures.
Furthermore, diethyl(phenylacetyl)malonate can be used in the production of organic molecules with rings, which are essential components 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 powerful building block in organic synthesis. Its unique reactivity profile allows for the construction of diverse molecular architectures across various chemical domains. This robust molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.