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Direct benzylic metalation of a phenethylamine derivative: potassium as the key to both generation and stabilization of a labile anion.

Chemical communications (Cambridge, England) (2012-09-21)
Christian Unkelbach, Hannah S Rosenbaum, Carsten Strohmann
ABSTRAKT

t-BuLi-t-BuOK selectively metalates the benzylic position of 2-phenylethyldimethylamine under mild conditions without occurrence of β-elimination in the resulting metalated species. Theoretical and structural studies indicate that potassium is crucial for both the lowering of the barrier of the initial deprotonation step and the stabilization of the labile anion.

MATERIAŁY
Numer produktu
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Opis produktu

Sigma-Aldrich
Phenethylamine, purified by redistillation, ≥99.5%
Sigma-Aldrich
Phenethylamine, ≥99%
Sigma-Aldrich
n-Butyllithium solution, 11.0 M in hexanes
Sigma-Aldrich
n-Butyllithium solution, 2.5 M in hexanes
Sigma-Aldrich
n-Butyllithium solution, 2.7 M in heptane
Sigma-Aldrich
n-Butyllithium solution, 2.0 M in cyclohexane
Sigma-Aldrich
n-Butyllithium solution, 1.6 M in hexanes