Abstract

The results for efficient tertiary and primary amine functionalization of polymeric organolithium compounds in hydrocarbon solution at room temperature are described for termination reactions with N-trimethylsilylbenzophenone imine, 3-dimethylaminopropyl chloride and 2,2,5,5-tetramethyl-1-(3-chloropropyl)-1-aza-2,5-disilacyclopentane. Functionalizations with the functionalized initiator, 2,2,5,5-tetramethyl-1-(3-lithiopropyl)-1-aza-2,5-disilacyclopentane are presented. Conditions for quantitative amine functionalization were observed for all of these reactions and reagents.

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