Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthetic organic molecule. It is a colorless to pale yellow liquid with a characteristic odor. This chemical reagent is widely used in research laboratories for its ability to form intermediates.
The structure of diethyl(phenylacetyl)malonate consists of a phenyl acetyl group attached to a diethyl malonate. This chemical arrangement allows it to engage in chemical synthesis.
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 production 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 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.
Characterization of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a substance with the chemical formula C15H18O4. This derivative can be prepared through several methods, often involving the reaction of phenylacetic acid with diethyl malonate. It exhibits distinct physical characteristics, such as a hue 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 uses in various synthetic processes.
- Additional research continues to explore its potential in the synthesis of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate possesses a distinct set of physicochemical properties that contribute its reactivity and applications. Its chemical formula, C16H18O4, reflects the presence of an array of ethyl ester groups and a phenylacetyl moiety. The material's molar mass is around 274.31 g/mol, indicating its moderate weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a liquid state with a distinctive odor. Its miscibility CAS 94-24-6 Tetracaine in common organic solvents remains to be limited. The compound's melting point shifts depending on purity and factors. Its boiling point, on the other hand, falls within a narrow range. The presence of reactive groups within its structure affects its atomic interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate plays a crucial function in organic chemistry due to its versatile composition. This material can be readily modified through various chemical processes to yield a wide collection of valuable products. For instance, diethyl(phenylacetyl)malonate can be utilized in the synthesis of drugs, agrochemicals, and other synthetic products.
One notable use is its role in the creation of esters with a beta-hydroxyl group, which are frequently employed as precursors in the formation of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be employed in the production of ring-containing compounds, which are essential parts 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 diverse molecular architectures across diverse chemical domains. This robust molecule serves as a valuable intermediate for the development of new pharmaceuticals, agrochemicals, and materials.