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

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
ABSTRACT

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.

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Sigma-Aldrich
n-Butillitio, 2.5 M in hexanes
Sigma-Aldrich
n-Butillitio, 1.6 M in hexanes
Sigma-Aldrich
n-Butillitio, 2.0 M in cyclohexane
Sigma-Aldrich
Phenethylamine, 99%
Sigma-Aldrich
2-Phenylethylamine hydrochloride, ≥98%
Sigma-Aldrich
n-Butillitio, 2.7 M in heptane
Sigma-Aldrich
n-Butillitio, 11.0 M in hexanes
Sigma-Aldrich
Phenethylamine, ≥99%
Sigma-Aldrich
Phenethylamine, purified by redistillation, ≥99.5%
Supelco
2-Phenethylamine, analytical standard