A Convenient Synthesis of 4-Aminomethyl-L-Phenylalanine

Abstract

N-Boc-4-Aminomethyl-L-phenylalanine is prepared from N-Boc-4-Iodophenylalanine in 78% yield over three steps. The method features an efficient Pd-catalyzed carbonylation, oxime formation, and subsequent catalytic reduction employing an ethanol/water/acetic acid solvent system which is crucial to successful reaction.