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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 1-Methylpiperazine | HCID 53167 | — |
| Edukt | 7-Nitro-2,3-dihydro-1,4-benzodioxine-5-carboxylic acid | HCID 12464533 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 5-[(4-Methyl-1-piperazinyl)-carbonyl]-7-nitro-1,4-benzodioxane | HCID 20544709 | 66,8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04255580 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-a6eaa157bbf84254bbbd0054b5218a67 |
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| Quellennotiz | uspto-grants-1981_03 |
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