Sodium Triacetoxyborohydride: Overview
Sodium triacetoxyborohydride (STAB) is a selective reducing agent commonly used in organic synthesis, particularly for the reductive amination of aldehydes and ketones with amines. It is milder than other reducing agents like sodium borohydride (NaBH₄) and is often preferred due to its selectivity and tolerance of a wide range of functional groups.
Chemical Structure and Properties
Chemical Name: Sodium triacetoxyborohydride
Molecular Formula: C₆H₁₀BNaO₆
Molecular Weight: 211.95 g/mol
CAS Number: 56553-60-7
Physical Properties:
Sodium triacetoxyborohydride is composed of a borohydride (BH₄) core stabilized by three acetoxy groups (-OCOCH₃), which reduce its reactivity compared to sodium borohydride. This modification allows the reagent to be more selective, especially in the presence of aldehydes, amines, and ketones.
Synthesis
Sodium triacetoxyborohydride is typically synthesized by reacting sodium borohydride (NaBH₄) with acetic acid or acetyl chloride. The reaction leads to the formation of the acetoxy groups that modify the borohydride, making it less reactive but still effective in selective reductions.
Key Applications
The reductive amination process with STAB follows these steps:
Advantages of Sodium Triacetoxyborohydride
Sodium triacetoxyborohydride (STAB) is a selective reducing agent commonly used in organic synthesis, particularly for the reductive amination of aldehydes and ketones with amines. It is milder than other reducing agents like sodium borohydride (NaBH₄) and is often preferred due to its selectivity and tolerance of a wide range of functional groups.
Chemical Structure and Properties
Chemical Name: Sodium triacetoxyborohydride
Molecular Formula: C₆H₁₀BNaO₆
Molecular Weight: 211.95 g/mol
CAS Number: 56553-60-7
Physical Properties:
| Property | Description |
|---|---|
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in acetonitrile, DMF, DCM; reacts with water |
| Melting Point | 116-120°C |
| Stability | Stable under dry conditions, decomposes in moist environments |
| Storage Conditions | Store in a cool, dry place away from moisture |
Synthesis
Sodium triacetoxyborohydride is typically synthesized by reacting sodium borohydride (NaBH₄) with acetic acid or acetyl chloride. The reaction leads to the formation of the acetoxy groups that modify the borohydride, making it less reactive but still effective in selective reductions.
Key Applications
- Reductive Amination: Sodium triacetoxyborohydride is predominantly used in reductive amination, a widely used method to form secondary and tertiary amines. In this reaction, an aldehyde or ketone reacts with a primary or secondary amine to form an imine intermediate, which is then reduced to form the desired amine.
Reaction Example: Aldehyde/Ketone+Amine+Sodium triacetoxyborohydride→Amine\text{Aldehyde/Ketone} + \text{Amine} + \text{Sodium triacetoxyborohydride} \rightarrow \text{Amine}Aldehyde/Ketone+Amine+Sodium triacetoxyborohydride→Amine
The mildness of STAB ensures that the imine is selectively reduced without over-reducing other functional groups, making it ideal for sensitive or complex molecules. - Selective Reduction of Imine and Iminium Ions: STAB is also widely used for the reduction of imines or iminium ions that are formed in situ during reactions. The reagent is preferred due to its selectivity in these reductions, avoiding the reduction of carbonyl compounds or esters that may be present in the molecule.
- Mild Reducing Agent: Compared to sodium borohydride or lithium aluminum hydride, STAB is much milder and therefore allows for selective reduction in the presence of various functional groups. It does not reduce esters, carboxylic acids, or amides, making it highly selective for aldehydes and ketones when other sensitive functional groups are present.
- Used in Drug Synthesis: Sodium triacetoxyborohydride is commonly used in the pharmaceutical industry for the synthesis of complex molecules, particularly in the development of amine-containing drugs. Its selectivity and ability to work under mild conditions make it a valuable reagent in medicinal chemistry.
The reductive amination process with STAB follows these steps:
- Formation of the Imine:
The aldehyde or ketone reacts with the amine to form an imine intermediate. In some cases, the imine can exist as an iminium ion, depending on the reaction conditions. - Reduction:
Sodium triacetoxyborohydride selectively reduces the imine or iminium ion to produce the amine. The acetoxyborohydride reacts with the imine to transfer hydride ions, facilitating the reduction.
Advantages of Sodium Triacetoxyborohydride
- Selective and Mild:
STAB is much more selective and milder than other reducing agents like sodium borohydride, lithium aluminum hydride, or even sodium cyanoborohydride. This makes it ideal for sensitive substrates where side reactions must be minimized. - No Cyanide Toxicity:
Unlike sodium cyanoborohydride, STAB is a safer alternative, as it does not release toxic cyanide ions. This is particularly advantageous in large-scale industrial applications. - Tolerates Functional Groups:
STAB selectively reduces imines without affecting other functional groups like esters, carboxylic acids, or amides, providing a high level of control in complex organic syntheses.