Cyanohydrin reaction

From Wikipedia, the free encyclopedia

A Cyanohydrin reaction is an organic reaction by an aldehyde or ketone with a cyanide anion or a nitrile to form a cyanohydrin. This nucleophilic addition is a reversible reaction but with aliphatic carbonyl compounds equilibrium is in favor of the reaction products. The cyanide source can be potassium cyanide, sodium cyanide or trimethylsilylcyanide. With aromatic aldehydes such as benzaldehyde the benzoin condensation is a competing reaction. The reaction is used in carbohydrate chemistry as a chain extension method for example that of D-xylose.

Reaction of acetone with sodium cyanide to hydroxyacetonitrile
Reaction of acetone with sodium cyanide to hydroxyacetonitrile
Reaction of benzoquinone with trimethylsilylcyanide, catalyst KCN is introduced as a 1:1 complex with the Crown ether 18-crown-6
Reaction of benzoquinone with trimethylsilylcyanide in tetrachloromethane, catalyst KCN is introduced as a 1:1 complex with the Crown ether 18-crown-6
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

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 alcoxy 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.


[edit] External links

[edit] References

  1. ^ 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 Abstract Support info plus proposed transition state
  2. ^ Urech, Ann. 164, 256 (1872)
Retrieved from "http://en.wikipedia.org../../../c/y/a/Cyanohydrin_reaction.html"