Diethyl(phenylacetyl)malonate, also recognized as more info chemical abstract service identifier 20320-59-6, is a laboratory chemical. It is a viscous colorless oil with a distinctive aroma. This chemical reagent is widely used in research laboratories for its ability to form intermediates.
The formula of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonic ester derivative. This molecular design 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 synthesis 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 reagent, 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 reaction.
- 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 produced through several methods, often involving the reaction of phenylacetic acid with diethyl malonate. It exhibits distinct physical attributes, such as a shade that ranges from colorless to light yellow and a temperature of around 270°C.
- Important structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found purposes in various organic processes.
- Additional research continues to explore its potential in the synthesis of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that determine its reactivity and applications. Its molecular formula, C16H18O4, reflects the presence of an array of ethyl ester groups and the phenylacetyl moiety. The material's molar mass is approximately 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a viscous state with a specific odor. Its dissolvability in common organic solvents is to be high. The compound's transition temperature varies depending on purity and factors. Its boiling point, on the other hand, falls within a narrow range. The presence of polar groups within its structure affects its intermolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate serves a crucial part in organic reactions due to its versatile composition. This material can be readily modified through various organic reactions to yield a wide range of valuable compounds. For illustration, diethyl(phenylacetyl)malonate can be employed in the preparation of pharmaceuticals, agrochemicals, and various organic materials.
One notable utilization is its role in the synthesis of beta-hydroxy esters, which are frequently employed as intermediates in the formation of complex compounds.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the synthesis 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 featuring a distinctive structure, has emerged as a versatile building block in organic synthesis. Its remarkable reactivity profile allows for the fabrication of elaborate molecular architectures across various chemical domains. This adaptable molecule serves as a valuable precursor for the development of new pharmaceuticals, agrochemicals, and materials.