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Lithium triethylborohydride is the organoboron compound with the formula LithiumEthyl groupBorohydride. Commonly referred to as LiTEBH or Superhydride, it is a powerful reducing agent used in organometallic and organic chemistry. It is a colorless or white liquid but is typically marketed and used as a THF solution. The related reducing agent sodium triethylborohydride is commercially available as toluene solutions.
LiBHEt3 is a stronger reducing agent than lithium borohydride and lithium aluminium hydride.
LiBHEt3 reduces a wide range of functional groups, but so do many other hydride reagents. Instead, LiBHEt3 is reserved for difficult substrates, such as sterically hindered carbonyls, as illustrated by reduction of 2,2,4,4-tetramethyl-3-pentanone. Otherwise, it reduces acid anhydrides to alcohols and the carboxylic acid, not to the diol. Similarly reduce to diols. α,β-Enones undergo 1,4-addition to give lithium . reduce to (via thiolates). LiBHEt3 deprotonates carboxylic acids, but does not reduce the resulting lithium carboxylates. For similar reasons, undergo ring-opening upon treatment with LiBHEt3 to give the alcohol. With unsymmetrical epoxides, the reaction can proceed with high regio- and stereo- selectivity, favoring attack at the least hindered position:
and are not reduced by LiBHEt3. It can be used in the reductive cleavage of mesylates and . LiBHEt3 can selectively deprotect tertiary N-acyl groups without affecting secondary amide functionality. It has also been shown to reduce aromatic esters to the corresponding alcohols as shown in eq 6 and 7.
LiBHEt3 also reduces pyridine and isoquinolines to piperidines and tetrahydroisoquinolines respectively.
The reduction of β-hydroxysulfinyl imines with catecholborane and LiBHEt3 produces anti-1,3-amino alcohols shown in (8).
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