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 distinctive aroma. 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 diethyl malonate. This unique structure allows it to participate in various reactions.
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 production 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 product can be prepared through several methods, often involving the reaction of phenylacetic acid with diethyl malonate. It exhibits characteristic physical properties, such as a shade that ranges from colorless to light yellow and a boiling 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 chemical transformations.
- Additional research continues to explore its potential in the creation of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a distinct set of physicochemical properties that contribute its reactivity and applications. Its chemical formula, C16H18O4, reflects the presence of two ethyl ester groups and a phenylacetyl moiety. The compound's molar mass is approximately 274.31 g/mol, indicating its considerable weight. At room temperature, diethyl(phenylacetyl)malonate exists as a solid state with a distinctive odor. Its solubility in common organic solvents remains to be high. The compound's transition temperature shifts depending on purity and conditions. Its boiling point, on the other hand, resides within a specific range. The presence of functional groups within its structure affects its intermolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial part in organic reactions due to its versatile composition. This material can be readily transformed through various synthetic processes to yield a wide range of valuable substances. For illustration, diethyl(phenylacetyl)malonate can be utilized in the preparation of drugs, pesticides, and other synthetic materials.
One notable use is its role in the creation of esters with a beta-hydroxyl group, which are commonly employed as precursors in the formation of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the creation of ring-containing compounds, which are essential cas 59-46-1 Procaine (base) components 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 versatile building block in organic synthesis. Its uncommon reactivity profile allows for the construction of diverse molecular architectures across numerous chemical domains. This flexible molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.