The Reactions of 3-Phenyl-1-butylamine-3-<sup>14</sup>C and 3-p-Anisyl-1-butylamine-3-<sup>14</sup>C with Nitrous Acid<sup>1,2</sup>
作者:Arthur W. Fort、Robert E. Leary
DOI:10.1021/ja01495a024
日期:1960.5
The diazotization of 3-phenyl-1-butylamine-3-C/sup 14/ in acetic acid gives 3-phenyl-1-butene, 3-phenyl-1-butyl acetate, and diastereoisomeric 3- phenyl-2-butyl acetates. 3-pmixture. The secondary ester products of these reactions show extensive isotope-position rearrangement. The significance of these results is discussed.
3-苯基-1-丁胺-3-C/sup 14/在乙酸中的重氮化得到3-苯基-1-丁烯、3-苯基-1-丁基乙酸酯和非对映异构的3-苯基-2-丁基乙酸酯。3-混合。这些反应的二级酯产物显示出广泛的同位素位置重排。讨论了这些结果的重要性。