116150-20-0 | (1-Acetylpyrrolidin-2-yl)boronic acid

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Description

• Catalog Number: AA15057
• Chemical Name: (1-Acetylpyrrolidin-2-yl)boronic acid
• CAS Number: 116150-20-0
• Molecular Formula: C6H12BNO3
• Molecular Weight: 156.9754
• MDL Number: MFCD18383203
• SMILES: OB(C1CCCN1C(=O)C)O

Upstream Synthesis Route

The (1-Acetylpyrrolidin-2-yl)boronic acid, commonly referred to as $name$, is a versatile chemical compound widely used in organic synthesis. It plays a crucial role as a boronic acid derivative in various chemical reactions, particularly in the field of organic chemistry.One of the key applications of $name$ in chemical synthesis is its ability to act as a valuable building block for Suzuki-Miyaura cross-coupling reactions. When utilized in these reactions, (1-Acetylpyrrolidin-2-yl)boronic acid serves as a coupling partner with aryl halides or pseudo-halides, leading to the formation of biaryl compounds. This reaction is highly significant in the assembly of complex organic molecules, especially in pharmaceutical and material science research.Moreover, (1-Acetylpyrrolidin-2-yl)boronic acid demonstrates remarkable versatility in forming carbon-carbon bonds through other coupling reactions such as Chan-Lam coupling, Sonogashira coupling, and Stille coupling. These synthetic methodologies highlight the importance of $name$ as a pivotal reagent in the construction of diverse organic structures with precision and efficiency.In addition to its role in cross-coupling reactions, (1-Acetylpyrrolidin-2-yl)boronic acid also functions as a ligand in organometallic chemistry, facilitating catalytic processes and promoting selective transformations. Its unique coordination properties enhance the catalytic activity of transition metals, enabling the synthesis of complex molecules with high stereochemical control.Overall, the application of $name$ in chemical synthesis underscores its significance as a versatile and indispensable compound in modern organic chemistry. Its diverse reactivity and compatibility with various reaction conditions make it a valuable tool for organic chemists in designing and executing complex synthetic pathways.