Diethyl(phenylacetyl)malonate, also recognized as CAS ID 20320-59-6, is a synthesized compound. It is a white crystalline solid with a characteristic odor. This chemical reagent is widely used in research laboratories for its ability to form intermediates.
The formula of diethyl(phenylacetyl)malonate consists of a phenylacetyl moiety attached to a malonic ester derivative. This unique structure allows it to undergo transformations.
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 primary 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, click here 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 ester can be prepared through several methods, often involving the reaction of phenylacetic acid with diethyl malonate. It exhibits distinct physical attributes, such as a hue that ranges from colorless to light yellow and a boiling point of around 270°C.
- Important structural features include the presence of two ethyl ester groups and a phenylacetyl group.
- Diethyl(phenylacetyl)malonate has found uses in various organic reactions.
- Additional research continues to explore its potential in the development of new compounds.
Physicochemical Properties of Diethyl(phenylacetyl)malonate
Diethyl(phenylacetyl)malonate possesses a distinct set of physicochemical properties that influence its reactivity and applications. Its chemical formula, C16H18O4, reflects the presence of an array of ethyl ester groups and one phenylacetyl moiety. The substance's molar mass is approximately 274.31 g/mol, indicating its substantial weight. At room temperature, diethyl(phenylacetyl)malonate retains as a liquid state with a characteristic odor. Its miscibility in common organic solvents remains to be limited. The compound's melting point shifts depending on purity and influences. Its boiling point, on the other hand, falls within a narrow range. The presence of polar groups within its structure impacts its atomic interactions.
Applications of Diethyl(phenylacetyl)malonate in Organic Chemistry
Diethyl(phenylacetyl)malonate serves a crucial part in organic synthesis due to its versatile composition. This material can be readily modified through various chemical transformations to yield a wide range of valuable compounds. For example, diethyl(phenylacetyl)malonate can be utilized in the preparation of pharmaceuticals, herbicides, and other organic products.
One notable use is its role in the production of beta-hydroxy esters, which are frequently employed as building blocks in the assembly of complex molecules.
Furthermore, diethyl(phenylacetyl)malonate can be utilized in the production of heterocyclic compounds, which are essential parts 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 potent building block in organic synthesis. Its uncommon reactivity profile allows for the construction of diverse molecular architectures across numerous chemical domains. This robust molecule serves as a valuable foundation for the development of new pharmaceuticals, agrochemicals, and materials.