Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthetic organic molecule. It is a white crystalline solid with a pungent smell. This organic compound is widely used in academic settings for its ability to serve as a precursor.
The formula of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonate diester. This chemical arrangement allows it to engage in chemical synthesis.
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 synthesis 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 subjected to malonic ester. The final product, diethyl(phenylacetyl)malonate, is obtained after a series of chemical transformations involving condensation.
- 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 derivative can be prepared through several methods, often involving the transformation of phenylacetic acid with diethyl malonate. It exhibits unique physical attributes, such as a color 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 purposes in various synthetic transformations.
- Further research continues to explore its potential in the development 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 multiple ethyl ester groups and one phenylacetyl moiety. The compound's molar mass is around 274.31 g/mol, indicating its considerable weight. At room temperature, diethyl(phenylacetyl)malonate exists as a solid state with a specific odor. Its solubility in common organic solvents remains to be high. The compound's melting point varies depending on purity and influences. Its boiling point, on the other hand, resides within a narrow range. The presence of functional groups within its structure impacts its intermolecular interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial role in organic reactions due to its versatile structure. This molecule can be readily transformed through various chemical transformations to yield a wide range of valuable products. For example, diethyl(phenylacetyl)malonate can be employed in the creation of drugs, herbicides, and other organic substances.
One notable utilization is its role in the production of esters with a beta-hydroxyl group, which are frequently employed as precursors in the formation of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be used in the production Cas 136-47-0 Tetracaine hcl of organic molecules with rings, which are essential components 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 construction of complex molecular architectures across numerous chemical domains. This robust molecule serves as a valuable intermediate for the development of new pharmaceuticals, agrochemicals, and materials.