During an effort to synthesize the trans-III-copper(II)-1,4,8,11-tetramethyl-pyro-phosphonate-1,4,8,11-tetra-aza-cyclo-tetradecane, using only metal perchlorate salts, it was noted that the perchlorate is reduced to chloride. This surprising result may be explained only by the fact that Cu2+(aq) catalyzes the reduction of perchlorate by formaldehyde or by H2. These reactions are slow at room temperature and ambient pressures. DFT calculations support the involvement of the transient CuH+ in the reduction process.