chain extension of D-xylose in equilibrium with its hemiacetal with KCN to the cyclic ester
chain extension of D-xylose in equilibrium with its hemiacetal with KCN to the cyclic ester
Reaction mechanism
Mechanism of the cyanohydrin reaction
Asymmetric synthesis
The asymmetric cyanohydrin reaction of benzaldehyde with trimethylsilylcyanide is made possible by employment of (R)-Binol[1] at 1 to 10% catalyst loading. This ligand firsts reacts with a lithium alkoxy compound to form a lithium binaphtholate Complex.
Asymmetric reaction of benzaldehyde with (R)-Binol-lithium(i-propyloxy) gives (S)-cyanohydrin with 98% ee
Asymmetric reaction of benzaldehyde with (R)-Binol-lithium(i-propyloxy) gives (S)-cyanohydrin with 98% ee
The chemist Urech in 1872 was the first to synthesize cyanohydrins from ketones with alkali cyanides and acetic acid [2] and therefore this reaction also goes by the name of Urech cyanohydrin method.
External links
Cyanohydrin reaction of formaldehyde to hydroxyacetonitrile or glycolonitrile with sodium cyanide in Organic Syntheses Coll. Vol. 2, p.387; Vol. 13, p.56 Article
↑Chiral Lithium Binaphtholate Aqua Complex as a Highly Effective Asymmetric Catalyst for Cyanohydrin Synthesis Manabu Hatano, Takumi Ikeno, Takashi Miyamoto, and Kazuaki Ishihara J. Am. Chem. Soc.; 2005; 127(31) pp 10776 - 10777 AbstractSupport info plus proposed transition state