Cyanohydrin reaction

From Wikipedia, the free encyclopedia
Jump to: navigation, search

A cyanohydrin reaction is an organic chemical 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 trimethylsilyl cyanide. 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 benzoquinone with trimethylsilylcyanide, catalyst KCN is introduced as a 1:1 complex with the Crown ether 18-crown-6

Reaction mechanism[edit]

Mechanism of the cyanohydrin reaction

Asymmetric synthesis[edit]

The asymmetric cyanohydrin reaction of benzaldehyde with trimethylsilylcyanide is made possible by employment of (R)-Binol[1] at 1–10% 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)-acetonitrile with 98% ee
Asymmetric reaction of benzaldehyde with (R)–Binol–lithium(i-propyloxy) gives (S)-acetonitrile 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. With HCN in acidic conditions – i.e. the cyanohydrin is the functional group CN–C–OH

External links[edit]


  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 10776–77 Abstract Support info plus proposed transition state
  2. ^ Urech, Ann. 164, 256 (1872)