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DOI: 10.1055/s-0029-1218269
2-Azido-1,3-dimethylimidazolinium Chloride: An Efficient Diazo Transfer Reagent for 1,3-Dicarbonyl Compounds
Publication History
Publication Date:
08 October 2009 (online)
Abstract
Diazo transfer from 2-azido-1,3-dimethylimidazolinium chloride to 1,3-dicarbonyl compounds has been developed. The reaction proceeds under mild conditions to give 2-diazo-1,3-dicarbonyl compounds in high yields, which are easily isolated because the by-products are highly soluble in water.
Key words
azides - diazo compounds - diazonium salt - diazo-transfer - heterocycles
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References and Notes
The formation of salt 2 was confirmed by mass spectral analysis. The FAB(positive) mass spectrum of the mixture of the chloroimidazorium salt 3 and sodium azide showed a peak at m/z = 140, which corresponds to the calculated mass of [2 - Cl-]+.
7Typical procedure: [Caution: Although we have never had any trouble with azidoimidazolinium salt 2 , it is potentially explosive.] To a solution of 2-chloro-1,3-dimethyl-imidazolinium chloride (3; 1.2 mmol) in acetonitrile (2 mL), sodium azide (1.2 mmol) was added at 0 ˚C and the mixture was stirred for 30 min. 1,3-Dicarbonyl compound (1.0 mmol) and triethylamine (2.0 mmol) in THF (4 mL) was added to the mixture, which was stirred until the 1,3-dicarbonyl compound was consumed (reaction monitored by TLC). The reaction was quenched with water, and organic materials were extracted three times with CH2Cl2. The combined extracts were washed with water and brine, and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo to afford the crude compound, which was almost pure. The crude materials were purified by flash column chromatography (silica gel: hexane-ethyl acetate) to give pure 2-diazo-1,3-dicarbonyl compound.