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 molecule is widely used in various industrial applications for its ability to form intermediates.
The composition of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonate diester. This unique structure 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 preparation of various complex molecules, particularly in the field of pharmaceuticals and agrochemicals. The synthesis typically involves a two-step process. In the first 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 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.
Characterization of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a compound with the chemical formula C15H18O4. This product can be prepared through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits characteristic physical characteristics, such as a shade that ranges from colorless to light yellow and a vaporization 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 uses in various synthetic processes.
- Further research continues to explore its potential in the creation of novel compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate exhibits a distinct set of physicochemical properties that determine its reactivity and applications. Its structural formula, C16H18O4, reflects the presence of multiple ethyl ester groups and the phenylacetyl moiety. The material's molar mass is approximately 274.31 g/mol, indicating its moderate weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a viscous state with a characteristic odor. Its solubility in common organic solvents remains to be high. The compound's solidus point fluctuates depending on purity and influences. Its boiling point, on the other hand, resides within a narrow range. The presence of reactive groups within its structure affects its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial part in organic reactions due to its versatile structure. This material can be readily modified through various synthetic transformations to yield a wide array of valuable compounds. For illustration, diethyl(phenylacetyl)malonate can be utilized in the creation of drugs, pesticides, and other chemical materials.
One notable application is its role in the production of beta-hydroxy esters, which are frequently Mol File: 20320-59-6.mol employed as precursors in the construction of complex structures.
Furthermore, diethyl(phenylacetyl)malonate can be employed in the production of organic molecules with rings, 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 powerful building block in organic synthesis. Its unique reactivity profile allows for the synthesis of diverse molecular architectures across numerous chemical domains. This flexible molecule serves as a valuable precursor for the development of new pharmaceuticals, agrochemicals, and materials.