HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1691932Erstellt: 26. Oktober 2026
p-Fluoronitrobenzene → Methyl 1-(4-nitrophenyl)piperidine-4-carboxylate
https://huagongshe.com/reaction/1691932
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Fluoronitrobenzene | HCID 9590 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Methyl isonipecotate | HCID 424914 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 1-(4-nitrophenyl)piperidine-4-carboxylate | HCID 345002 | 37,4% |
Reaktionsschritte
To a solution of 4-fluoronitrobenzene (0.70 g, 4.96 mmol) in THF (8 mL) was added piperadine-4-carboxylic acid methyl ester (0.71 g, 4.96 mmol) and diisopropylethylamine (0.66 g, 5.11 mmol). The mixture was heated in a microwave oven at 150° C. for 1.5 hr. The resulting mixture was extracted with ethyl acetate and hydrochloric acid (0.2 N). The organic layer was washed with brine and concentrated sodium bicarbonate solution. After the evaporation of solvents, the residue was purified through a Biotage flash column chromatography using ethyl acetate and hexanes (1:1 ratio) to give a yellow solid as 1-(4-nitrophenyl)-piperidine-4-carboxylic acid methyl ester (490 mg). 1H-NMR is consistent with the structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08153644B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-2e91b16b27d145648a4b459fad382340 |
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| Quellennotiz | uspto-grants-2012_04 |
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