HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 586775Erstellt: 24. Oktober 2026
Potassium Carbonate → Tert-butyl 4-(3-nitrophenyl)piperazine-1-carboxylate
https://huagongshe.com/de/reaction/586775
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Edukt | 1-Fluoro-3-nitrotoluene | HCID 69422064 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | Tert-butyl 4-(3-nitrophenyl)piperazine-1-carboxylate | HCID 22330126 | 413,6% |
Reaktionsschritte
5.0 g (3.54 mmol) of 1-fluoro-3-nitrotoluene, 9.89 g (5.31 mmol) of tert-butyl 1-piperazinecarboxylate and 27.0 g (19.5 mmol) of potassium carbonate are solubilized under an argon atmosphere in DMSO (60 ml), then the reaction medium is taken to 100° C. for 72 hours. The reaction medium is then cooled down using an ice bath then poured into ice-cold water. The product is extracted using 3 times 50 ml of dichloromethane. The organic solution is dried over magnesium sulphate, followed by filtration and concentration under vacuum. Purification on a silica column is then carried out (eluent=heptane 70%/ethyl acetate 30%) in order to produce a yellow solid. The yellow solid is further purified by recrystallization from diisopropyl ether in order to produce 4.5 g of the expected product (yield 42.0%). Melting point: 82.0-92.0° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06936715B2 |
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| Quelldatensatz | uspto-grants-2005_08 |
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| ORD ID | ord-1fbf293717524a70880adf47e1cd8373 |
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| Quellennotiz | uspto-grants-2005_08 |
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