19.3: Reductions using NaBH4, LiAlH4

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Reduction of aldehydes and ketones

The most common sources of the hydride nucleophile are lithium aluminium hydride (LiAlH₄) and sodium borohydride (NaBH₄). Note! The hydride anion is not present during this reaction; rather, these reagents serve as a source of hydride due to the presence of a polar metal-hydrogen bond. Because aluminium is less electronegative than boron, the Al-H bond in LiAlH₄ is more polar, thereby, making LiAlH₄ a stronger reducing agent. 19.3.jpeg

Addition of a hydride anion (H:^–) to an aldehyde or ketone gives an alkoxide anion, which on protonation yields the corresponding alcohol. Aldehydes produce 1º-alcohols and ketones produce 2º-alcohols. 19.3-image.jpeg

In metal hydrides reductions the resulting alkoxide salts are insoluble and need to be hydrolyzed (with care) before the alcohol product can be isolated. In the sodium borohydride reduction the methanol solvent system achieves this hydrolysis automatically. In the lithium aluminium hydride reduction water is usually added in a second step. The lithium, sodium, boron and aluminium end up as soluble inorganic salts at the end of either reaction. Note! LiAlH₄ and NaBH₄ are both capable of reducing aldehydes and ketones to the corresponding alcohol.

Examples

Mechanism

This mechanism is for a LiAlH₄ reduction. The mechanism for a NaBH₄ reduction is the same except methanol is the proton source used in the second step.

1) Nucleophilic attack by the hydride anion

2) The alkoxide is protonated

Going from Reactants to Products Simplified

Properties of hydride sources

Two practical sources of hydride-like reactivity are the complex metal hydrides lithium aluminium hydride (LiAlH₄) and sodium borohydride (NaBH₄). These are both white (or near white) solids, which are prepared from lithium or sodium hydrides by reaction with aluminum or boron halides and esters. Lithium aluminium hydride is by far the more reactive of the two compounds, reacting violently with water, alcohols and other acidic groups with the evolution of hydrogen gas. The following table summarizes some important characteristics of these useful reagents.

Exercises

1) Please draw the products of the following reactions:

2) Please draw the structure of the molecule which must be reacted to produce the product.

3) Deuterium oxide (D₂O) is a form of water where the hydrogens have been replaced by deuteriums. For the following LiAlH₄ reduction the water typically used has been replaced by deuterium oxide. Please draw the product of the reaction and place the deuterium in the proper location. Hint! Look at the mechanism of the reaction.

Answers

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Contributors

Prof. Steven Farmer (Sonoma State University)
William Reusch, Professor Emeritus (Michigan State U.), Virtual Textbook of Organic Chemistry

Alcohols from carbonyl compounds: Reduction

Aldehydes, ketones and alcohols are very common features in biological molecules. Converting between these compounds is a frequent event in many biological pathways. However, semi-anionic compounds like sodium borohydride don’t exist in the cell. Instead, a number of biological hydride donors play a similar role.

NADH is a common biological reducing agent. NADH is an acronym for nicotinamide adenine dinucleotide hydride. Insetad of an anionic donor that provides a hydride to a carbonyl, NADH is actually a neutral donor. It supplies a hydride to the carbonyl under very specific circumstances. In doing so, it forms a cation, NAD⁺. However, NAD⁺ is stabilized by the fact that its nicotinamide ring is aromatic; it was not aromatic in NADH.

Reduction of carboxylic acids and esters

Carboxylic acids can be converted to 1^o alcohols using Lithium aluminium hydride (LiAlH₄). Note that NaBH₄ is not strong enough to convert carboxylic acids or esters to alcohols. An aldehyde is produced as an intermediate during this reaction, but it cannot be isolated because it is more reactive than the original carboxylic acid.

Esters can be converted to 1^o alcohols using LiAlH₄, while sodium borohydride ($$NaBH_4$$) is not a strong enough reducing agent to perform this reaction.