Reacción #214616
ord-391e3988e0a84fcd9b479b48e55c37b0
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
10°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroprovided with an agitator
- 2Temperaturabeing maintained below 20° C
- 3OtroAfter agitation of the mixture, the crystals were dried off
- 4Lavadowashed with methylethylcetone
- 5Otrodried
- 6workup.DISSOLUTIONdissolved in water
- 7Otroreprecipitated by addition of 50 ml of 20% ammonia
- 8OtroThe crystals were dried off
- 9Lavadowashed with water
- 10Otrodried
Procedimiento
400 ml of methylethylacetone and 11 g of methylpiperazine were introduced into a balloon flask provided with an agitator and a thermometer. The mixture was cooled to 10° C. and then 41 g of 6,7-dibromo-8-nitro-1,4-benzodioxane-5-carbonyl chloride were added in portions with the temperature being maintained below 20° C. After agitation of the mixture, the crystals were dried off, washed with methylethylcetone and dried and then dissolved in water and reprecipitated by addition of 50 ml of 20% ammonia. The crystals were dried off, washed with water and dried. 33 g of 5-[(4-methyl-1-piperazinyl)-carbonyl]-6,7-dibromo-8-nitro-1,4-benzodioxane were obtained (M.P: 164° C.; yield: 69.6%).