Herein, we report our findings on the novel ability of
aluminum
chloride (AlCl<sub>3</sub>) in fluorinated solvent 1,1,1,3,3,3-hexafluoroisopropanol
[HFIP] to selectively deprotect the <i>N</i>-benzyloxycarbonyl
group (<i>N</i>-Cbz). The salient features of this method
are good functional group tolerance including other reducible groups,
cost-effectiveness, easy-to-handle, safe protocol, amenable to scale-up,
high yields, and ambient temperature reactions. The methodology would
serve as an excellent alternative to the use of pyrophoric hydrogen
gas and metal catalyst reagents that pose severe safety and environmental
concerns. The most notable feature of this methodology is the orthogonal
deprotection of the <i>N</i>-Cbz group in the presence of <i>O</i>- and <i>N</i>-Bn protecting groups, hence, expanding
the scope for designing synthetic routes to target compounds requiring
multiple functional group transformations.