Research

On the kinetic and thermodynamic reactivity of lithium Di(alkyl)amidozincate bases in directed ortho metalation


Reference:

Kondo, Y., Morey, J. V., Morgan, J. C., Naka, H., Nobuto, D., Raithby, P. R., Uchiyama, M. and Wheatley, A. E. H., 2007. On the kinetic and thermodynamic reactivity of lithium Di(alkyl)amidozincate bases in directed ortho metalation. Journal of the American Chemical Society, 129 (42), pp. 12734-12738.

Related documents:

This repository does not currently have the full-text of this item.
You may be able to access a copy if URLs are provided below.

Abstract

Sequential reaction of HTMP (= 2,2,6,6-tetramethylpiperidine) with (BuLi)-Bu-n and Et2Zn affords unsolvated polymer chains of EtZn(mu-Et)(mu-TMP)Li 6. The scope of this reagent in directed ortho metalation (DoM) chemistry has been tested by its reaction with N,N-diisopropylnaphthamide in THF to give EtZn(mu-C10H6C(O)(NPr2)-Pr-j-2)(2)Li center dot 2THF 7. Data reveal that 6 has undergone reaction with 2 equiv of aromatic tertiary amide and imply that it exhibits dual alkyl/amido basicity. DFT calculations reveal that direct alkyl basicity is kinetically disfavored and instead point to a stepwise mechanism whereby 6 acts as an amido base, liberating HTMP during the first DoM event. Re-coordination of the amine at lithium then incurs the elimination of EtH. Reaction of the resulting alkyl(amido)(arylamido)zincate with a second equivalent of N,Ndiisopropylnaphthamide eliminates HTMP and affords 7. Both DoM steps involve the exhibition of amido basicity and each reveals a low kinetic barrier to reaction. Understanding of this reaction sequence is tested by treating 6 with N,N-diisopropylbenzamide in THF. On the basis of theory and experiment, the presence of THF solvent (in place of stronger Lewis bases) combined with the use of a sterically less congested aromatic amide is expected to encourage threefold, stepwise reaction. Isolation and characterization of the resulting tripodal zincate Zn(mu-C6H4C(O)(NPr2)-Pr-j-2)(3)Li center dot THF 8 bears this out and suggests a significant new level of control in zincate-induced DoM chemistry through the combination of experiment and DFT studies.

Details

Item Type Articles
CreatorsKondo, Y., Morey, J. V., Morgan, J. C., Naka, H., Nobuto, D., Raithby, P. R., Uchiyama, M. and Wheatley, A. E. H.
DOI10.1021/ja072118m
DepartmentsFaculty of Science > Chemistry
RefereedYes
StatusPublished
ID Code4585
Additional InformationID number: ISI:000250327000057

Export

Actions (login required)

View Item