L-Dipivaloyltartaric acid
[CAS# 65259-81-6]

Identification

• Classification: Chemical reagent >> Organic reagent >> Fatty acid
• Name: L-Dipivaloyltartaric acid
• Synonyms: (2R,3R)-2,3-Bis(2,2-dimethyl-1-oxopropoxy)butanedioic acid
• Molecular Formula: C₁₄H₂₂O₈
• Molecular Weight: 318.32
• CAS Registry Number: 65259-81-6
• SMILES: CC(C)(C)C(=O)O[C@H]([C@H](C(=O)O)OC(=O)C(C)(C)C)C(=O)O

Properties

• Solubility: Very slightly soluble (0.8 g/L) (25 ºC), Calc.^*
• Density: 1.240±0.06 g/cm³ (20 ºC 760 Torr), Calc.^*
• Melting point: 127-132 ºC (Expl.)
• Index of Refraction: 1.484, Calc.^*
• Boiling Point: 436.6±45.0 ºC (760 mmHg), Calc.^*
• Flash Point: 153.8±22.2 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2014 ACD/Labs)

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H302-H315-H319-H335
• Precautionary Statements: P261-P305+P351+P338

Discovory and Applicatios

L-Dipivaloyltartaric acid, also known as L-DPTA, is a chemical compound derived from tartaric acid. It is a derivative where two pivaloyl groups (C5H9O2) are attached to the hydroxyl groups of the tartaric acid molecule. Tartaric acid itself is a naturally occurring organic acid found in many plants, particularly in grapes, and plays a role in wine production. The modification of tartaric acid by introducing pivaloyl groups to form L-DPTA has led to significant interest in its applications, particularly in the field of asymmetric synthesis and catalysis.

The discovery and synthesis of L-DPTA can be traced back to efforts aimed at developing chiral ligands and catalysts for use in enantioselective reactions. In the early 1980s, the importance of tartaric acid derivatives in catalysis was recognized, especially due to the chiral nature of tartaric acid, which makes it useful in producing enantiomerically pure compounds. The modification of tartaric acid to create derivatives like L-DPTA allowed for the development of more efficient and selective catalytic processes, as pivaloyl groups can provide steric bulk and enhance the chiral recognition in various reactions.

L-Dipivaloyltartaric acid finds its primary use in asymmetric synthesis, a branch of chemistry concerned with the selective production of one enantiomer over another in chiral molecules. In this context, L-DPTA is employed as a chiral auxiliary or ligand in catalysis, where its ability to form complexes with metal ions helps direct the formation of specific enantiomers in chemical reactions. This has made L-DPTA an important compound in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where chirality is critical.

The role of L-DPTA in catalysis is particularly evident in the development of asymmetric reactions, such as asymmetric hydrogenation and asymmetric oxidation. It is used as a ligand in the preparation of chiral metal complexes, which can catalyze reactions that yield enantiomerically pure products. These reactions are essential in the production of drugs and other biologically active compounds, where the presence of a specific enantiomer is often crucial for efficacy and safety.

L-Dipivaloyltartaric acid has also been used in the synthesis of chiral polymers and materials. The use of L-DPTA as a chiral building block allows for the creation of materials with distinct optical properties, which can be applied in areas such as optoelectronics and material science. Additionally, its potential as a stabilizing agent in various chemical processes has made it a subject of ongoing research.

In summary, L-Dipivaloyltartaric acid is a modified form of tartaric acid with two pivaloyl groups attached. It plays a significant role in asymmetric synthesis, particularly in catalysis, where it is used as a chiral auxiliary or ligand in the preparation of chiral metal complexes. Its applications are most notable in the production of enantiomerically pure compounds, which are essential in the pharmaceutical and chemical industries. The continued development and use of L-DPTA in synthetic chemistry contribute to advances in enantioselective processes and the synthesis of complex molecules.

References

2022. Synthesis of P- and S-Stereogenic Compounds via Enantioselective C-H Functionalization. Synthesis, 54(14).
DOI: 10.1055/a-1802-6793

2007. Asymmetric Protonation. Kalesse, M. Science of Synthesis, 25, 148.

2005. With a Chiral Proton Source. Plaquevent, J.-C.; Cahard, D.; Guillen, F. Science of Synthesis, 26, 502.