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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127434Erstellt: 25. Oktober 2026

1-Methylpiperazine → 5-[(4-Methyl-1-piperazinyl)-carbonyl]-6,7-dibromo-8-nitro-1,4-benzodioxane

https://huagongshe.com/reaction/127434

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-MethylpiperazineHCID 53167—
Edukt6,7-Dibromo-8-nitro-1,4-benzodioxane-5-carbonyl chlorideHCID 20544755—
Lösungsmittel3-Methylpentan-2-OneHCID 11262—
Produkt5-[(4-Methyl-1-piperazinyl)-carbonyl]-6,7-dibromo-8-nitro-1,4-benzodioxaneHCID 2054474269,6%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04255580
Quelldatensatzuspto-grants-1981_03
ORD IDord-391e3988e0a84fcd9b479b48e55c37b0
Quellennotizuspto-grants-1981_03