反应详情

To a solution of 3-methyl-1-trichloromethyl-2-butenyl acetoacetate (5.75 g, 0.02 mole) and triethylamine (2.02 g, 0.02 mole) in 50 ml of acetonitrile was added a solution of tosyl azide (3.94 g, 0.02 mole, prepared according to the method of Organic Synthesis Collective Volume V, page 179 A) in acetonitrile dropwise over a period of 10 minutes. The resultant mixture, containing the thus produced 3-methyl-1-trichloromethyl-2-butenyl-2-diazoacetoacetate, was stirred at room temperature for two hours and then poured into 60 ml (0.06 mole) of 1 N aqueous sodium hydroxide. The resulting mixture was stirred at room temperature for 30 minutes and then extracted with about 100 ml of ether. After phase separation, the aqueous layer was extracted with an additional 150 ml portion of ether, and the ether extracts were combined. The ethereal solution was then washed ten times with 50 ml portions of 3% aqueous potassium hydroxide containing sodium chloride and then three times with 50 ml portions of saturated aqueous sodium chloride. The washed ethereal solution was dried over magnesium sulfate, and the ether was removed by evaporation, affording a brown oily residue. The residue was purified by column chromatography on silica gel using benzene as the eluant, to give 3-methyl-1-trichloromethyl-2-butenyl diazoacetate (4.63 g, 85% yield).

1. customprepared
2. stirringThe resulting mixture was stirred at room temperature for 30 minutes
3. extractionextracted with about 100 ml of ether
4. customAfter phase separation
5. extractionthe aqueous layer was extracted with an additional 150 ml portion of ether
6. washThe ethereal solution was then washed ten times with 50 ml portions of 3% aqueous potassium hydroxide
7. additioncontaining sodium chloride
8. dry with materialThe washed ethereal solution was dried over magnesium sulfate
9. customthe ether was removed by evaporation
10. customaffording a brown oily residue
11. customThe residue was purified by column chromatography on silica gel