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According to retro-synthetic analyses and the literature, 2,6 both methyl 2-oxo-2-arylacetate and methyl 2- hydroxyimino-2-arylacetate 2 are the key intermediates of the analogues of strobilurins. Our initial goal was to develop a new method for synthesis of methyl 2- oxo-2-arylacetate in which the commercially available and cheap arylamines and glyoxylic acid were used as starting material based on previous literature.10,11 In our work, we first found that the coupling reaction between aryldiazonium salt derived from 2-methylaniline and methyl 2-(hydroxyimino)-acetate gave stereoselectively oxime 2 in 44% yield.12 The E/Z ratio determined in the crude mixture by 1H NMR spectroscopy was ca. 14:1. After further column chromatography purification, the purity of E-2 could exceed 99% in41% yield. The compound E-2 was methylated by sodium hydride-dimethyl sulfate in 91% yield and successively brominated with NBS to afford oxime ether 4 in 81% yield. |
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