Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a laboratory chemical. It is a colorless to pale yellow liquid with a characteristic odor. This molecule is widely used in academic settings for its ability to react with other compounds.
The composition of diethyl(phenylacetyl)malonate consists of a phenylacetyl moiety attached to a malonic ester derivative. This unique structure allows it to participate in various reactions.
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 production 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 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 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.
Description of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a substance with the chemical formula C15H18O4. This product can be produced through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits characteristic physical characteristics, read more such as a shade that ranges from colorless to light yellow and a boiling 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 chemical reactions.
- Further research continues to explore its potential in the creation of novel compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that influence its reactivity and applications. Its chemical formula, C16H18O4, reflects the presence of multiple ethyl ester groups and a phenylacetyl moiety. The material's molar mass is roughly 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate preserves as a liquid state with a specific odor. Its solubility in common organic solvents proves to be limited. The compound's transition temperature varies depending on purity and factors. Its boiling point, on the other hand, resides within a determined range. The presence of functional groups within its structure impacts its intramolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial role in organic synthesis due to its versatile arrangement. This molecule can be readily altered through various organic transformations to yield a wide collection of valuable substances. For instance, diethyl(phenylacetyl)malonate can be used in the preparation of drugs, pesticides, and diverse synthetic substances.
One notable use is its role in the synthesis of esters with a beta-hydroxyl group, which are often employed as intermediates in the construction of complex structures.
Furthermore, diethyl(phenylacetyl)malonate can be used in the synthesis of ring-containing compounds, which are essential components 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 remarkable reactivity profile allows for the construction of diverse molecular architectures across various chemical domains. This robust molecule serves as a valuable precursor for the development of new pharmaceuticals, agrochemicals, and materials.