tert-butyl trans-3-hydroxy-4-methoxypyrrolidine-1-carboxylate CAS:148214-86-2

As a versatile building block, this molecule facilitates efficient medicinal chemistry and materials synthesis. Reactions at the pyrrolidine nitrogen systematically introduce diversity enabling focused library creation. Additionally, conversions of the alcohol furnish varied esters and ethers. These transformations produce targeted collections of compounds applicable to pharmaceutical research and development. The tert-butyl group supports improved solubility and stability. It may further serve as a monomer for specialty polymer synthesis. Moreover, the alcohol and methoxy sites render this suitable for surface functionalization and coatings development. Therefore, with multiple reactive handles, this synthon enables versatile synthesis of drugs, functional biomaterials and other value-added chemicals through strategic manipulations.