Aluminum trifluoromethanesulfonate
[CAS# 74974-61-1]

Identification

• Classification: Organic raw materials >> Organometallic compound >> Organic aluminum
• Name: Aluminum trifluoromethanesulfonate
• Synonyms: Aluminum triflate
• Molecular Formula: C₃AlF₉O₉S₃
• Molecular Weight: 474.19
• CAS Registry Number: 74974-61-1
• EC Number: 629-179-9
• SMILES: C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[Al+3]

Properties

• Melting point: 300 ºC (Expl.)

Safety Data

• Hazard Symbols: GHS05 Danger
• Hazard Statements: H314
• Precautionary Statements: P260-P264-P280-P301+P330+P331-P302+P361+P354-P304+P340-P305+P354+P338-P316-P321-P363-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin corrosion	Skin Corr.	1B	H314
Serious eye damage	Eye Dam.	1	H318

• Transport Information: UN 3261

Discovory and Applicatios

Aluminum trifluoromethanesulfonate (AlOTf) is a highly effective Lewis acid that has garnered significant attention for its diverse applications in organic synthesis and catalysis. The compound is composed of an aluminum center coordinated with three trifluoromethanesulfonate (OTf) ligands, which are strong electron-withdrawing groups. This unique structure imparts strong Lewis acidity to the molecule, enabling it to catalyze a variety of reactions that involve electron-rich species. The discovery of AlOTf can be traced back to the study of aluminum-based Lewis acids, which have long been used to facilitate reactions such as Friedel–Crafts acylation and alkylation.

The development of aluminum trifluoromethanesulfonate emerged from the quest for more powerful and selective Lewis acids, especially in the context of electrophilic activation of substrates. Early works in this area focused on modifying aluminum salts to enhance their catalytic activity without compromising stability or selectivity. The introduction of the trifluoromethanesulfonate group proved to be a successful strategy, as it significantly increased the electron-accepting ability of the aluminum center, making it more efficient in catalyzing a wide range of reactions.

Aluminum trifluoromethanesulfonate is widely used in various organic reactions, particularly those that require mild yet effective Lewis acid catalysis. One of the key applications of AlOTf is in the catalysis of reactions involving carbon-carbon bond formation, such as the Diels–Alder reaction. In this reaction, AlOTf helps activate the dienophile by enhancing its electrophilicity, thereby promoting the formation of cyclohexene derivatives. The compound is also employed in reactions like acylation, alkylation, and esterification, where its strong Lewis acidity facilitates the formation of reactive intermediates, enabling the synthesis of complex organic molecules.

In addition to its role in organic synthesis, aluminum trifluoromethanesulfonate has found applications in the field of materials science. Its strong Lewis acidity makes it a useful catalyst for the polymerization of various monomers, particularly those that are difficult to polymerize under conventional conditions. AlOTf has also been investigated for its ability to initiate the polymerization of lactones, which is a key step in the production of biodegradable polyesters. Furthermore, the compound’s stability under various reaction conditions makes it a valuable tool for synthesizing novel polymeric materials with specific properties, such as high thermal stability or chemical resistance.

The versatility of aluminum trifluoromethanesulfonate extends to its use in the synthesis of chiral compounds, where it has been employed in asymmetric catalysis. Its ability to promote selective reactions in the presence of a variety of substrates has led to the development of new catalytic systems for the synthesis of optically active molecules. This application is particularly important in the pharmaceutical industry, where the demand for enantiomerically pure compounds is high.

Overall, aluminum trifluoromethanesulfonate is a powerful and versatile Lewis acid with a wide range of applications in organic synthesis, catalysis, and materials science. Its unique ability to activate electron-rich substrates makes it an invaluable tool in the development of novel chemical processes and the synthesis of complex molecules.

References

2024. Role of ion pairs in model glycosylation reactions of permethylated glucosyl and xylosyl triflates. Carbohydrate Research, 544.
DOI: 10.1016/j.carres.2024.109227

2022. A Facile Synthesis of 2-Oxazolines via Dehydrative Cyclization Promoted by Triflic Acid. Molecules (Basel, Switzerland), 27(24).
DOI: 10.3390/molecules27249042

1981. Deglycosylation of glycoproteins by trifluoromethanesulfonic acid. Analytical Biochemistry, 117(2).
DOI: 10.1016/0003-2697(81)90168-8