A Study of the Alkylation of 2-Phenylbutanenitrile with Butyl Chlorides1
GL GOERNER, AA HOLZSCHUH
Index: Goerner; Holzschuh Journal of Organic Chemistry, 1958 , vol. 23, p. 1346,1348
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Abstract
2-Phenylbutanenitrile has been alkylated with the butyl chlorides, using both sodamide and sodium hydride as condensing agents. With sodium hydride, the yields of products were found to be from 3 to 15y0 less than with sodamide. As predicted on the basis of Newman's
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