58901-83-0Relevant articles and documents
REACTION OF 4-SUBSTITUTED BENZALDEHYDES AND ACETOPHENONES WITH CHLOROACETONITRILE
Svoboda, Jiri,Kocfeldova, Zuzana,Palecek, Jaroslav
, p. 822 - 832 (2007/10/02)
Under conditions of phase-transfer catalysis or in homogeneous solution of potassium tert-butoxide the title compounds give stereoisomeric mixtures of substituted 2,3-epoxy nitriles III and IV.Alkaline hydrolysis of epoxy nitriles IV afforded the corresponding 2-arylpropanals in low yields.On treatment with methanol and potassium carbonate, epoxy nitriles III and IV were converted into epoxy esters in good yields.
Process for preparing glycidonitriles
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, (2008/06/13)
Process for preparing glycidonitriles in which a ketone or aldehyde is reacted with chloroacetonitrile under substantially anhydrous conditions using inorganic alkali metal bases in a solvent medium containing at least about 3 percent liquid volume of a dipolar, aprotic liquid such as dimethylformamide, any balance of solvent being a nonpolar organic liquid.