Chemistry:Lithium triethylborohydride
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| Names | |
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| Preferred IUPAC name
Lithium triethylboranuide | |
| Other names
Superhydride
LiTEBH | |
| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
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PubChem CID
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| Properties | |
| Li(C2H5)3BH | |
| Molar mass | 105.95 g/mol |
| Appearance | Colorless to yellow liquid |
| Density | 0.890 g/cm3, liquid |
| Boiling point | 66 °C (151 °F; 339 K) for THF |
| reactive | |
| Hazards | |
| Main hazards | highly flammable corrosive Causes burns Probable Carcinogen |
| Safety data sheet | External MSDS |
| GHS pictograms |   
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| GHS Signal word | Danger |
| H250, H260, H314, H335 | |
| P210, P222, P223, P231+232, P260, P261, P264, P271, P280, P301+330+331, P302+334, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P335+334, P363, P370+378, P402+404, P403+233, P405, P422, P501 | |
| NFPA 704 (fire diamond) | |
| Related compounds | |
Related hydride
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Lithium borohydride sodium borohydride sodium hydride lithium aluminium hydride |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Lithium triethylborohydride is the organoboron compound with the formula LiEt3BH. 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.[2] 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.
Preparation
LiBHEt3 is prepared by the reaction of lithium hydride (LiH) and triethylborane (Et3B) in tetrahydrofuran (THF):
- LiH + Et3B → LiEt3BH
Its THF solutions are stable indefinitely in the absence of moisture and air.
Reactions
Alkyl halides are reduced to the alkanes by LiBHEt3.[3][4][2]
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 lactones reduce to diols. α,β-Enones undergo 1,4-addition to give lithium enolates. Disulfides reduce to thiols (via thiolates). LiBHEt3 deprotonates carboxylic acids, but does not reduce the resulting lithium carboxylates. For similar reasons, epoxides 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:
Acetals and ketals are not reduced by LiBHEt3. It can be used in the reductive cleavage of mesylates and tosylates.[5] LiBHEt3 can selectively deprotect tertiary N-acyl groups without affecting secondary amide functionality.[6] 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.[7]
The reduction of β-hydroxysulfinyl imines with catecholborane and LiBHEt3 produces anti-1,3-amino alcohols shown in (8).[8]
Precautions
LiBHEt3 reacts exothermically, potentially violently, with water, alcohols, and acids, releasing hydrogen and the pyrophoric triethylborane.[2]
References
- ↑ "Lithium triethylhydroborate" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/23712863#section=Safety-and-Hazards.
- ↑ 2.0 2.1 2.2 Zaidlewicz, M.; Brown, H.C. (2001). "Lithium Triethylborohydride". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons. doi:10.1002/047084289X.rl148. ISBN 0471936235. https://doi.org/10.1002/047084289X.rl148.pub2. Retrieved 2022-02-18.
- ↑ Marek Zaidlewicz; Herbert C. Brown (2001). "Lithium Triethylborohydride". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rl148. ISBN 0471936235.
- ↑ Brown, H. C.; Kim, S. C.; Krishnamurthy, S. (1980-02-01). "Selective reductions. 27. Reaction of alkyl halides with representative complex metal hydrides and metal hydrides. Comparison of various hydride reducing agents". J. Org. Chem. 45 (5): 849–856. doi:10.1021/jo01293a018. https://pubs.acs.org/doi/10.1021/jo01293a018. Retrieved 2022-02-18.
- ↑ Baer, H.H.; Mekarska-Falicki, M. (November 1985). "Stereochemical dependence of the mechanism of deoxygenation, with lithium triethylborohydride, in 4,6-O-benzylidenehexopyranoside p-toluenesulfonates". Canadian Journal of Chemistry 63 (11): 3043. doi:10.1139/v85-505. https://doi.org/10.1139/v85-505. Retrieved 2022-02-18.
- ↑ Tanaka, H.; Ogasawara, K. (2002-06-17). "Utilization oh lithium triethylborohydride as a selective N-acyl deprotecting agent". Tetrahedron Lett. 43 (25): 4417. doi:10.1016/S0040-4039(02)00844-4. https://doi.org/10.1016/S0040-4039(02)00844-4. Retrieved 2022-02-18.
- ↑ Blough, B.E.; Carroll, F.I. (1993-11-05). "Reduction of isoquinoline and pyridine-containing heterocycles with lithium triethylborohydride (Super-Hydride®)". Tetrahedron Lett. 34 (45): 7239. doi:10.1016/S0040-4039(00)79297-5. https://www.sciencedirect.com/science/article/abs/pii/S0040403900792975. Retrieved 2022-02-18.
- ↑ Kochi, T.; Tang, T.P.; Ellman, J.A. (2002-05-14). "Asymmetric Synthesis of syn- and anti-1,3-Amino Alcohols". J. Am. Chem. Soc. 124 (23): 6518–6519. doi:10.1021/ja026292g. PMID 12047156. https://doi.org/10.1021/ja026292g. Retrieved 2022-02-18.
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