Diethyl (Phenylacetyl) Malonate CAS 20320-59-6

Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthesized compound. It is a viscous colorless oil with a characteristic odor. This molecule is widely used in academic settings for its ability to react with other compounds.

The structure of diethyl(phenylacetyl)malonate consists of a phenyl acetyl group attached to a malonate diester. This chemical arrangement allows it to engage in chemical synthesis.

Chemical Synthesis of Diethyl(phenylacetyl)malonate

The synthesis 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 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 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 ester can be synthesized through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits distinct physical characteristics, such as a shade 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 purposes in various synthetic processes.
  • Further research continues to explore its potential in the development of novel compounds.

Physicochemical Properties of Diethyl(phenylacetyl)malonate

Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that contribute its reactivity and applications. Its structural formula, C16H18O4, reflects the presence of two ethyl ester groups and one phenylacetyl moiety. The substance's molar mass is roughly 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate retains as a viscous state with a characteristic odor. Its miscibility in common organic solvents is to be moderate. The compound's melting point fluctuates depending on purity and factors. Its boiling point, on the other hand, resides within a narrow range. The presence of polar groups within its structure affects its atomic interactions.

Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry

Diethyl(phenylacetyl)malonate serves a crucial part in organic chemistry due to its versatile composition. This material can be readily altered through various organic transformations to yield a wide range of valuable substances. For instance, diethyl(phenylacetyl)malonate can be used in the synthesis of pharmaceuticals, agrochemicals, and diverse synthetic substances.

One notable utilization is its role in the production of esters with a beta-hydroxyl group, which cas 5337-93-9 4-Methylpropiophenone are often employed as precursors in the construction of complex molecules.

Furthermore, diethyl(phenylacetyl)malonate can be employed in the creation of heterocyclic 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 possessing a distinctive structure, has emerged as a powerful building block in organic synthesis. Its unique 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.

Leave a Reply

Your email address will not be published. Required fields are marked *