58477-04-6

Upstream product

• 140-29-4 phenylacetonitrile 

Downstream Products

• 89237-30-9 phenyl-1'cyano-1'dimethyl-2,3 cyclopentanone 
• 89237-30-9 phenyl-1'cyano-1'dimethyl cyclopentanone 
• 106325-21-7 ((1R,2S)-3-Oxo-2-phenyl-cyclohexyl)-phenyl-acetonitrile 
• 106325-21-7 ((1S,2S)-3-Oxo-2-phenyl-cyclohexyl)-phenyl-acetonitrile 
• 827-36-1 2-(N,N-dimethylamino)-2-phenylacetonitrile 

Relevant academic research and scientific papers

Study of the lithiated phenylacetonitrile monoanions and dianions formed according to the lithiated base used (LHMDS, LDA, or n-BuLi). 1. Evidence of heterodimer ( Quadac ) or dianion formation by vibrational spectroscopy

It is evidenced through vibrational spectroscopy that a heterodimer or Quadac is formed when an excess of base (LHMDS, LDA, or n-BuLi) is added to PhCH2CN in THF, THF-hexane, or THF-toluene solution. The amount of heterodimer increases with the pKHa of the lithiated base. A dianionic species may be formed through decomposition of this heterodimer if the pKHa of the base is sufficiently high, as in the case of n-BuLi. With LDA, only a very small amount of dianion is observed, and with LHMDS, no dianion is detected. The predominant dianionic species observed are the linear and bridged separated ion pairs of the dilithiated dianion. The presence of the amine in the medium is of paramount importance. The PhCHCNLi monomer-dimer equilibrium is entropy driven toward the dimer solvated by the amine.