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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127419Erstellt: 25. Oktober 2026

Acetone → 5-[(4-Methyl-1-piperazinyl)-carbonyl]-7-nitro-1,4-benzodioxane

https://huagongshe.com/reaction/127419

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktWaterHCID 962—
Edukt1-MethylpiperazineHCID 53167—
Edukt7-Nitro-2,3-dihydro-1,4-benzodioxine-5-carboxylic acidHCID 12464533—
LösungsmittelTriethylamineHCID 8471—
Produkt5-[(4-Methyl-1-piperazinyl)-carbonyl]-7-nitro-1,4-benzodioxaneHCID 2054470966,8%

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

22 ml of water, 22.5 g of 7-nitro-1,4-benzodioxane-5-carboxylic acid, 65 ml of acetone and 10.5 g of triethylamine were introduced into a 250 ml balloon flask provided with an agitator and a thermometer. The mixture was cooled to 10° C. and then 14 g of isobutyl chloroformiate was added. The mixture was agitated and the temperature allowed to rise. The oily compound formed was cooled to 20° C., 11 g of N-methyl piperazine was added and then the mixture was agitated, allowing the temperature to rise. The crystals formed were washed with water. 20.5 g of 5-[(4-methyl-1-piperazinyl)-carbonyl]-7-nitro-1,4-benzodioxane was produced (M.P.: 218° C.; yield: 66.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04255580
Quelldatensatzuspto-grants-1981_03
ORD IDord-a6eaa157bbf84254bbbd0054b5218a67
Quellennotizuspto-grants-1981_03