Lithiation and substitution of N′ -(ω-phenylalkyl)-N,N- dimethylureas

Lithiation of N-phenethyl-N,N-dimethylurea with three equivalents of tert-butyllithium in anhydrous tetrahydrofuran at -78°C takes place on the nitrogen and on the side-chain of the CHnext to the phenyl ring (α-lithiation). The 2-lithio isomer can be obtained via bromine-lithium exchange of N-2-(2-bromophenyl)ethyl-N,N-dimethylurea using methyllithium followed by tert-butyllithium in tetrahydrofuran at -78°C. The lithium reagents thus obtained react with various electrophiles to give the corresponding substituted derivatives in excellent yields. Lithiation of N-(3-phenylpropyl)-N,N-dimethylurea takes place on the α-CHwith tert-butyllithium at 0 °C. On the other hand, lithiation of N-(4-phenylbutyl)-N,N-dimethylurea with tert-butyllithium at 0 °C takes place on one of the methyl groups of the urea unit.