Lithium triamylborohydride
[CAS# 60217-34-7]

Identification

• Classification: Organic raw materials >> Organometallic compound >> Organic lithium
• Name: Lithium triamylborohydride
• Synonyms: LS-Selectride
• Molecular Formula: C₁₅H₃₄B^.Li
• Molecular Weight: 232.18
• CAS Registry Number: 60217-34-7
• EC Number: 804-124-3
• SMILES: [Li+].[B-](C(C)C(C)C)(C(C)C(C)C)C(C)C(C)C

Properties

• Density: 0.903 g/mL (25 ºC) (Expl.)

Safety Data

• Hazard Symbols: GHS02;GHS08;GHS05;GHS07 Danger
• Hazard Statements: H225-H260-H314-H335-H336-H351
• Precautionary Statements: P210-P231+P232-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin corrosion	Skin Corr.	1B	H314
Substances or mixtures which in contact with water emit flammable gases	Water-react.	1	H260

Discovory and Applicatios

Lithium triamylborohydride is an organoboron reagent used primarily as a selective reducing agent in organic synthesis. It is composed of a lithium cation paired with the triamylborohydride anion, where the boron atom is bonded to three amyl groups (pentyl groups) and one hydride ion. The bulky amyl substituents create significant steric hindrance around the boron center, which influences the reagent's reactivity and selectivity. Its chemical formula is often represented as Li\[BH(Amy)₃], where Amy stands for the amyl group (–CH₂CH₂CH₂CH₂CH₃).

This reagent was developed to offer milder and more selective hydride reductions compared to traditional agents such as lithium aluminum hydride or sodium borohydride. Lithium triamylborohydride reduces functional groups like esters, lactones, and nitriles efficiently, often under milder conditions and with improved selectivity, making it valuable for complex organic synthesis where control over reduction is critical.

The introduction of bulky amyl groups was aimed at modulating the reagent’s steric and electronic properties, thus tuning its reducing power. This modification results in lower reactivity toward certain functional groups such as ketones and aldehydes, allowing selective reduction in multifunctional molecules.

In synthetic applications, lithium triamylborohydride is used to reduce esters to the corresponding alcohols without over-reduction, a common challenge with stronger hydride reagents. It can also selectively reduce acid chlorides to aldehydes, a useful transformation in organic synthesis for obtaining aldehydes that are sensitive to harsher conditions.

The reagent is typically handled as a solution in ethers such as tetrahydrofuran (THF) or diethyl ether, which stabilize the reactive hydride species. It is sensitive to moisture and air and must be stored and manipulated under inert atmosphere conditions to prevent decomposition and loss of activity. Contact with water or protic solvents results in rapid hydrogen gas evolution.

Safety precautions are necessary when working with lithium triamylborohydride due to its reactivity. Proper protective equipment such as gloves, goggles, and use of a fume hood are standard to avoid exposure and mitigate risks associated with its flammability and vigorous reaction with moisture.

Overall, lithium triamylborohydride is a valuable reagent for chemists seeking selective reduction pathways in complex molecule synthesis. Its unique steric profile allows precise control over hydride transfer reactions, contributing to advancements in pharmaceutical, agrochemical, and fine chemical manufacturing.

References

1978. Selective Reductions Using Metal Hydrides. Aspects of Mechanism and Organometallic Chemistry.
DOI: 10.1007/978-1-4684-3393-7_7

2005. Trialkylborohydrides. Science of Synthesis.
URL: https://science-of-synthesis.thieme.com/app/text/?id=SD-006-00975

2024. Synthetic techniques for thermodynamically disfavoured substituted six-membered rings. Nature Reviews Chemistry, 8(7).
DOI: 10.1038/s41570-024-00612-3