Amine diazotization, in situ nucleophilic aromatic substitution and [3+2] cycloaddition reaction of azide compound

SyntheticPage 411
Published May 26, 2010


Reaction Scheme

Procedure

To a cold solution of p-anisidine (10 g, 80 mmol) in hydrochloric acid (2 mol/L, 100 mL) was added sodium nitrite (6.3g, 91mmol) dissolved in water (25 mL) dropwise. After being stirred for 30 min at the same temperature, sodium azide (5.4 g, 83 mmol) dissolved in water (25 mL) was added dropwise and the mixture was stirred for one h. The solution was diluted with toluene (50 mL). The organic phase separated was dried over sodium sulfate, filtered and washed with toluene (50 mL). To the filtrate was added ethanol (100 mL), ethyl acetoacetate (10mL, 80 mmol) and sodium hydride (5g, 60% dispersion, 125 mmol) portionwise. After being stirred for 20 h at 80 oC, the mixture was evaporated. Hydrochloric acid (2 mol/L, 100 mL) was added to the residue and precipitated solid was filtered, washed with water (100 mL) and dried in vacuo to give the product (15.4 g, 40 mmol, 50%).

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