Diethyl (Phenylacetyl) Malonate CAS 20320-59-6
Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a laboratory chemical. It is a viscous colorless oil with a pungent smell. 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 malonic ester derivative. This chemical arrangement allows it to undergo transformations.
Chemical Synthesis of Diethyl(phenylacetyl)malonate
The get more info 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 reagent, such as sulfuric acid. This reaction yields phenyl acetate ester, which is then subjected 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 substance with the chemical formula C15H18O4. This derivative can be synthesized through several methods, often involving the reaction of phenylacetic acid with diethyl malonate. It exhibits unique physical characteristics, such as a shade that ranges from colorless to light yellow and a temperature of around 270°C.
- Significant structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found applications in various synthetic processes.
- Additional research continues to explore its potential in the development of novel compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate exhibits a distinct set of physicochemical properties that influence its reactivity and applications. Its structural formula, C16H18O4, reflects the presence of an array of ethyl ester groups and the phenylacetyl moiety. The compound'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 distinctive odor. Its solubility in common organic solvents remains to be limited. The compound's melting point fluctuates depending on purity and conditions. Its boiling point, on the other hand, resides within a determined range. The presence of reactive groups within its structure affects its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate serves a crucial role in organic reactions due to its versatile composition. This compound can be readily altered through various synthetic reactions to yield a wide range of valuable substances. For instance, diethyl(phenylacetyl)malonate can be utilized in the synthesis of drugs, pesticides, and various chemical substances.
One notable application is its role in the creation of alcohols with an ester group, which are often employed as precursors in the construction of complex compounds.
Furthermore, diethyl(phenylacetyl)malonate can be used in the creation 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 versatile building block in organic synthesis. Its uncommon reactivity profile allows for the fabrication of elaborate molecular architectures across diverse chemical domains. This robust molecule serves as a valuable intermediate for the development of new pharmaceuticals, agrochemicals, and materials.