Sodium triacetoxyborohydride
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Sodium triacetoxyborohydride
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CAS No:
56553-60-7
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Formula:
C6H10BO6.Na
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Chemical Name:
Sodium triacetoxyborohydride
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Synonyms:
Borate(1-),tris(acetato-κO)hydro-,sodium (1:1),(T-4)-;Borate(1-),tris(acetato-O)hydro-,sodium,(T-4)-;Borate(1-),tris(acetato-κO)hydro-,sodium,(T-4)-;Hydride,boron complex;Sodium triacetoxyborohydride;Sodium triacetoxy(hydro)borate;Sodium triacetatohydroborate;Sodium borohydride acetate;824402-68-8;1799649-67-4
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CAS No:
Characteristics
78.90000
-0.60710
White Powder
116-120 °C (dec.)(lit.)
Solubility in water: reaction.;soluble in dimethyl sulfoxide, methanol, benzene, toluene, terahydrofuran, dioxane and methylene chloride.
Flammables + water-Freezer (-20°C)e area
Safety Information
III
4.3
UN 1409 4.3/PG 2
3
15-34-14/15-37/38-11
43-7/8-45-36/37/39-26
F,Xi,C
Irritant/Flammable
Reacts violently with water.
Sodium triacetoxyborohydride Use and Manufacturing
Sodium Triacetoxyborohydride(STAB) is a hydride reagent used in stereoselective reductive amination. It is able to replace toxic sodium cyanoborohydride under most conditions. It is selective in reducing aldehydes to alcohols in the presence of ketones. STAB is also stable in anhydrous acids, which enables reductive amination of aldehydes and ketones. It used in reductive amination of ketones and aldehydes and reductive amination/lactamization of carbonyl compounds with amines. Reagent for the reductive amination of aryl aldehydes.The advantage of STAB compared to sodium cyanoborohydride is evident. STAB, being non-toxic, is easier to handle and forms no toxic by-products, making the treatment of process waste after the reaction simple and less costly. Selective reducing agent in organic synthesis. Sodium triacetoxyborohydride is especially suitable for reductive aminations. Since the reaction rate for the reduction of iminium ions is much faster than for ketones or even aldehydes, the reductive amination can be carried out as a one-pot procedure by introducing the reducing agent into a mixture of the amine and carbonyl compound. The presence of a stoichiometric amount of acetic acid, which catalyzes the imine formation and provides the iminium ion, doesn't present any problem under these conditions. Reductive amination (simplified)
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