Diethyl(phenylacetyl)malonate, also recognized as CAS registry number 20320-59-6, is a laboratory chemical. It is a white crystalline solid with a pungent smell. This molecule is widely used in various industrial applications for its ability to react with other compounds.
The structure of diethyl(phenylacetyl)malonate consists of a phenylacetyl moiety attached to a diethyl malonate. This unique structure allows it to participate in various reactions.
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 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 catalyst, 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 condensation.
- 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 derivative can be prepared through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits distinct physical properties, such as a shade that ranges from colorless to light yellow and a boiling 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 purposes in various organic processes.
- More research continues to explore its potential in the development of innovative compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that contribute its reactivity and applications. Its chemical formula, C16H18O4, reflects the presence of cas 14769-73-4 levamisole two ethyl ester groups and a phenylacetyl moiety. The compound's molar mass is approximately 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a solid state with a distinctive odor. Its miscibility in common organic solvents proves to be high. The compound's solidus point shifts depending on purity and influences. Its boiling point, on the other hand, falls within a specific range. The presence of polar groups within its structure contributes its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate serves a crucial function in organic chemistry due to its versatile composition. This molecule can be readily altered through various organic transformations to yield a wide collection of valuable compounds. For instance, diethyl(phenylacetyl)malonate can be used in the preparation of pharmaceuticals, pesticides, and other organic materials.
One notable utilization is its role in the synthesis of beta-hydroxy esters, which are frequently employed as precursors in the assembly of complex structures.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the synthesis 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 powerful building block in organic synthesis. Its unique reactivity profile allows for the fabrication of complex molecular architectures across various chemical domains. This robust molecule serves as a valuable intermediate for the development of new pharmaceuticals, agrochemicals, and materials.