Diethyl(phenylacetyl)malonate, also recognized as CAS registry number 20320-59-6, is a synthesized compound. It is a white crystalline solid with a distinctive aroma. This molecule is widely used in research laboratories for its ability to form intermediates.
The structure of diethyl(phenylacetyl)malonate consists of a acylated phenyl ring attached to a malonic ester derivative. This unique structure allows it to engage in chemical synthesis.
Chemical Synthesis of Diethyl(phenylacetyl)malonate
The preparation 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 initial cas 5337-93-9 4-Methylpropiophenone 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 subjected 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.
Description of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate is a molecule with the chemical formula C15H18O4. This derivative can be produced through several methods, often involving the transformation 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.
- 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.
- More research continues to explore its potential in the synthesis of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate exhibits a distinct set of physicochemical properties that contribute its reactivity and applications. Its molecular formula, C16H18O4, reflects the presence of an array of ethyl ester groups and one phenylacetyl moiety. The substance's molar mass is roughly 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate exists as a viscous state with a characteristic odor. Its miscibility in common organic solvents proves to be high. The compound's solidus point shifts depending on purity and influences. Its boiling point, on the other hand, falls within a narrow range. The presence of reactive groups within its structure impacts its atomic interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate acts a crucial part in organic chemistry due to its versatile structure. This compound can be readily transformed through various chemical processes to yield a wide array of valuable compounds. For instance, diethyl(phenylacetyl)malonate can be employed in the preparation of medicines, pesticides, and various synthetic substances.
One notable application is its role in the production of beta-hydroxy esters, which are frequently employed as building blocks in the construction of complex structures.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the production of organic molecules with rings, which are essential elements 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 remarkable reactivity profile allows for the fabrication of diverse molecular architectures across various chemical domains. This robust molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.