214973
Diisobutylaluminum hydride solution
1.0 M in methylene chloride
Synonym(s):
DIBAL, DIBAL-H
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About This Item
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form
liquid
Quality Level
reaction suitability
reagent type: reductant
concentration
1.0 M in methylene chloride
density
1.23 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
CC(C)C[AlH]CC(C)C
InChI
1S/2C4H9.Al.H/c2*1-4(2)3;;/h2*4H,1H2,2-3H3;;
InChI key
AZWXAPCAJCYGIA-UHFFFAOYSA-N
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General description
Diisobutylaluminum hydride is a reducing agent for many functional groups commonly used in organic synthesis.
Application
Diisobutylaluminum hydride solution (1 M in dichloromethane) has been used in the conversion of esters into α-fluoro-α,β-unsaturated esters in the presence of fluorocarboalkoxy-substituted dialkyl phosphonate anions via Horner-Wadsworth-Emmons reaction. It can be used in the multi-step synthesis of (S)-2-methyl tetrahydropyridine-N-oxide, a key structural moiety of bio-active compounds like himbacine and solenopsin-A.
Used in Pd-catalyzed reductive debromination of secondary alkyl bromides. O-Debenzylation and ring opening of perbenzylated furanosides. Convenient in situ generation of HZrCp2Cl from ZrCp2Cl2 and DIBAL-H.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Carc. 2 - Eye Dam. 1 - Pyr. Liq. 1 - Skin Corr. 1B - STOT SE 3 - Water-react 1
Target Organs
Central nervous system
Supplementary Hazards
Storage Class Code
4.2 - Pyrophoric and self-heating hazardous materials
WGK
WGK 2
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Diisobutylaluminum Hydride.
e-EROS Encyclopedia of Reagents for Organic Synthesis (2008)
Reduction-olefination of esters: a new and efficient synthesis of. alpha.-fluoro. alpha.,. beta.-unsaturated esters.
The Journal of Organic Chemistry, 55(15), 4639-4642 (1990)
An enantioselective route to trans-2, 6-disubstituted piperidines
Tetrahedron, 53(32), 11203-11210 (1997)
Reaction of diisobutylaluminum hydride with selected organic compounds containing representative functional groups
The Journal of Organic Chemistry, 50(14), 2443-2450 (1985)
The Journal of organic chemistry, 75(3), 627-636 (2009-12-31)
A systematic investigation of the reductive ring-expansion reaction of cyclic ketoximes fused to aromatic rings with diisobutylaluminum hydride (DIBALH) is described. This reaction regioselectively afforded a variety of five- to eight-membered bicyclic heterocycles or tricyclic heterocycles containing nitrogen neighboring an
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