Reacción #1545430

Ecuación de reacción

4-methoxyimino-5-methyl-6-(1-ethyl-5-hydroxypyrazol-4- yl) carbonylthiochroman-1,1-dioxide

phenacyl bromide

potassium carbonate

→

Compound 26

4-methoxyimino -5-methyl-6-(1- ethyl -5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide

Disolventes

acetone

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaunder heat for 8 hours
2. 2
   OtroInsolubles were removed by filtration
3. 3
   workup.DISTILLATIONthe acetone was distilled off
4. 4
   workup.DISSOLUTIONThe remainder was dissolved in ethyl acetate
5. 5
   Lavadothe resultant solution was washed with a saturated sodium chloride aqueous solution
6. 6
   Secadodried over anhydrous sodium sulfate
7. 7
   workup.DISTILLATIONThe ethyl acetate was distilled off under reduced pressure

Procedimiento

0.4 Gram (1.1 mmol) of 4-methoxyimino-5-methyl-6-(1-ethyl-5-hydroxypyrazol-4- yl) carbonylthiochroman-1,1-dioxide, 0.23 g (1.2 mmol) of phenacyl bromide and 0.15 g of potassium carbonate were added to 10 ml of acetone, and the mixture was stirred under heat for 8 hours. Insolubles were removed by filtration, and then the acetone was distilled off. The remainder was dissolved in ethyl acetate, and the resultant solution was washed with a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and the remainder was subjected to column chromatography (hexane/ethyl acetate) to give intended 4-methoxyimino -5-methyl-6-(1- ethyl -5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound 26) at a yield of 52%.

Fuente