HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 618376Erstellt: 24. Oktober 2026
Sodium Carbonate → 1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidine
https://huagongshe.com/de/reaction/618376
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 1-Chloro-4-fluoro-2-nitrobenzene | HCID 67659 | — |
| Edukt | 2,5-Difluoronitrobenzene | HCID 67767 | — |
| Edukt | Ethyl 4-amino-1-piperidinecarboxylate | HCID 100867 | — |
| Lösungsmittel | Cyclohexanol | HCID 7966 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Ethyl acetate hexane | HCID 21226206 | — |
| Produkt | 1-Ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)piperidine | HCID 13792162 | — |
Reaktionsschritte
A solution of ethyl 4-amino-1-piperidine carboxylate (9.0 g, 52 mmol.) and 2-chloro-5-fluoronitrobenzene (10.3 g, 58 mmol.) in cyclohexanol (30 mL) containing powdered sodium carbonate (6.1 g, 57 mmol.) was refluxed (>160° C.) for 30 hours or until no further reaction was indicated by tlc (30% EtOAc/hexane). (Alternatively, 2,5-difluoro-nitrobenzene can be used in place of the 2-chloro-5-fluoronitro-benzene). The deep reddish reaction mixture was cooled and diluted with EtOAc. This solution was washed with dil. aq. HCl (3×), water, and then the organic layer dried (anhydrous Na2SO4) and the solvent evaporated to give a red oil. This oil was flash chromatographed on a column of silica gel and the product eluted with a 10-25% EtOAc/hexane gradient. The appropriate fractions were combined, the solvents evaporated, and the residue triturated with 10% Et2O/hexane to give 1-ethoxycarbonyl-4-(4-fluoro-2-nitroanilino)-piperidine as a bright reddish-orange solid, mp: 115-116° C., which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05952351 |
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| Quelldatensatz | uspto-grants-1999_09 |
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| ORD ID | ord-331122e00e5b48ee96ad24e8a426d6ae |
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| Quellennotiz | uspto-grants-1999_09 |
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