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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-FluoronitrobenzeneHCID 9590—
EduktDiisopropylethylamineHCID 81531—
EduktMethyl isonipecotateHCID 424914—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 1-(4-nitrophenyl)piperidine-4-carboxylateHCID 34500237,4%

Reaktionsbedingungen

Temperatur150 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08153644B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-2e91b16b27d145648a4b459fad382340
Quellennotizuspto-grants-2012_04