The aggregation of BuLi (LiR) in diethyl ether (Et2O) in the presence of LiBr was studied by 6Li‐ and 13C‐NMR spectroscopy. For a 1.0 : 0.8 mixture of both species, the clusters (LiR)4, Li4R3Br, Li4R2Br2, Li4RBr3, and/or Li2RBr in the ratio 7 : 81 : 12 with Li4RBr3 and/or Li2RBr<1 were detected with the isotopic fingerprint method that is based on secondary deuterium (D)‐induced isotope shifts for δ(Li). The raising content of bromide ions causes increased shielding for δ(Li). As in the case of a 1 : 1 MeLi/LiBr mixture in Et2O, cluster Li4R3Br is the most stable one. In the presence of N,N,N′,N′‐tetramethylethylenediamine (TMEDA), only a mixed dimer was found. For LiClO4, no inclusion of the ClO$\rm{{_{4}^{-}}}$ ion could be detected. A mixture BuLi/PhLi 1 : 1 in Et2O in the presence of TMEDA showed only dimers with the mixed dimer as the most stable cluster. Chemical exchange of Li between the two homodimers was detected by EXSY spectroscopy. This implies an exchange mechanism with a fluxional tetramer as intermediate.