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1,1'-Bi-2-naphthol (BINOL) is an organic compound that is often used as a ligand for transition-metal catalysed asymmetric synthesis. BINOL has axial chirality and the two enantiomers can be readily separated and are stable toward racemisation. The specific rotation of the two enatiomers is +/- 35.5° (c=1 in THF). It is a precursor for another chiral ligand called BINAP.
Additional recommended knowledge
Racemic BINOL can also be produced using iron(III) chloride as an oxidant. The mechanism involves complexation of iron(III) into the hydroxyl, followed by a radical coupling reaction of the naphthol rings initiated by iron(III) oxidizing into iron(II).
Optically active BINOL can also be obtained from racemic BINOL by optical resolution. In one method, the alkaloid N-benzylcinchonidinium chloride form a crystalline inclusion compound. The inclusion compound of the S-enantiomer is soluble in acetonitrile but that of the R-enantiomer is not.
In another method BINOL is reacted with the acid chloride pentanoyl chloride to obtain the di-ester compound. The enzyme cholesterol esterase is then added in the form of bovine pancreas acetone powder which is able to hydrolyse the (S)-di-ester but not the (R)-di-ester. The (R)-dipentanoate is hydrolysed in a second step with sodium methoxide.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "1,1'-Bi-2-naphthol". A list of authors is available in Wikipedia.|