Litcius/Paper detail

Breaking the <i>tert</i> -Butyllithium Contact Ion Pair: A Gateway to Alternate Selectivity in Lithiation Reactions

Michael P. Crockett, Jeanette Piña, Achyut Ranjan Gogoi, Rémy F. Lalisse, Andrew Nguyen, Osvaldo Gutiérrez, Andy A. Thomas

2023Journal of the American Chemical Society21 citationsDOIOpen Access PDF

Abstract

The effects of Lewis basic phosphoramides on the aggregate structure of t- BuLi have been investigated in detail by NMR and DFT methods. It was determined that hexamethylphosphoramide (HMPA) can shift the equilibrium of t- BuLi to include the triple ion pair ( t -Bu–Li– t -Bu) − /HMPA 4 Li + which serves as a reservoir for the highly reactive separated ion pair t -Bu – /HMPA 4 Li + . Because the Li-atom’s valences are saturated in this ion pair, the Lewis acidity is significantly decreased; in turn, the basicity is maximized which allowed for the typical directing effects within oxygen heterocycles to be overridden and for remote sp 3 C–H bonds to be deprotonated. Furthermore, these newly accessed lithium aggregation states were leveraged to develop a simple γ-lithiation and capture protocol of chromane heterocycles with a variety of alkyl halide electrophiles in good yields.

Topics & Concepts

ChemistryElectrophileDeprotonationLithium (medication)Lewis acids and basesMedicinal chemistryComputational chemistryAlkylIonStereochemistryOrganic chemistryCatalysisEndocrinologyMedicineCoordination Chemistry and OrganometallicsAsymmetric Synthesis and CatalysisSynthesis and characterization of novel inorganic/organometallic compounds