(4R-cis)-6-Chloromethyl-2,2-dimethyl-1,3-dioxane-4-acetic Acid tert-Butyl Ester CAS:154026-94-5

The 4-position of the dioxane ring is substituted with a tert-butyl ester group, which is a bulky protecting group that provides protection for the carboxylic acid moiety. This protection is crucial during the synthesis and modification of the compound, as it prevents unwanted side reactions that might occur at the carboxylic acid site. At the 6-position, a chloromethyl group is attached. Chlorine is a halogen atom that can be involved in various chemical reactions, such as nucleophilic substitution. The presence of the chloromethyl group also suggests that this compound might be a useful intermediate for further functionalization, leading to the synthesis of more complex molecules. The (4R-cis) configuration indicates the stereochemistry at the 4-position, which is an important aspect of the compound's biological activity. Stereochemistry plays a crucial role in the way molecules interact with biological systems, and the (4R-cis) configuration may be significant for the compound's recognition by biological targets. The synthesis of (4R-cis)-6-chloromethyl-2,2-dimethyl-1,3-dioxane-4-acetic acid tert-butyl ester involves a series of organic reactions, including the formation of the 1,3-dioxane ring and the introduction of substituents at the specified positions. Careful control of reaction conditions is necessary to ensure the correct stereochemistry and to obtain the desired product with high purity and yield. This compound is likely to be of interest in the fields of organic synthesis and medicinal chemistry, as it can be used as a building block for the synthesis of more complex molecules, such as pharmaceutical agents or biologically active compounds. Its unique structure and protected functional groups make it a valuable intermediate for the development of new drugs and the study of biological processes.