X-ray crystallographic studies and comparative reactivity studies of a sodium diisopropylamide (NDA) complex and related hindered amides
X-ray crystallographic studies and comparative reactivity studies of a sodium diisopropylamide (NDA) complex and related hindered amides
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DOI:
10.1016/0022-328x(96)06203-1
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发表时间:
1996-07-12
影响因子:
2.3
通讯作者:
Wakefield, BJ
中科院分区:
文献类型:
--
作者:
Andrews, PC;Barnett, NDR;Wakefield, BJ
Two related sodium amide complexes derived from secondary amines with bulky organic substituents have been synthesised and crystallographically characterised. Both [(Pr-i)(2)NNa(TMEDA)](2) and [Cy(Pr-i)NNa(TMEDA)](2) adopt dimeric crystal structures with a central, planar (nitrogen-metal)(2) azametallocycle, a now familiar feature in both lithium amide and sodium amide chemistry. TMEDA ligands chelate in their usual bidentate manner making the Na+ cations four-coordinate with a distorted tetrahedral geometry. In the latter complex, the amido substituents are disposed in a trans conformation with respect to the (NNa)(2) ring plane. The deprotonating ability of the former complex has been tested against that of the parent amide [(Pr-i)(2)NNa](infinity) and the lithium congener [(Pr-i)(2)NLi](infinity) (LDA) in a series of simple organic reactions: selective enolate formation from 2-octanone and 2-methylcyclohexanone; synthesis of diphenylacetic acid via diphenylmethane. In general, the performance of the sodium reagents compares favourably with that of the lithium reagent.