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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2410294Erstellt: 26. Oktober 2026

Dimethylformamide → 1-(4-Chloro-2-nitrophenyl)piperidine

https://huagongshe.com/reaction/2410294

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2,5-DichloronitrobenzeneHCID 6977—
EduktPiperidineHCID 8082—
LösungsmittelWaterHCID 962—
Produkt1-(4-Chloro-2-nitrophenyl)piperidineHCID 28531896,4%

Reaktionsschritte

Piperidine (660 μl, 6.66 mmol, commercially available product) was added at room temperature to an N,N-dimethylformamide (DMF; 1 ml) solution of 1,4-dichloro-2-nitrobenzene (390 mg, 2.03 mmol, commercially available product). The resulting mixture was stirred for 18.5 hours. Water was added to the mixture, and the resulting mixture was extracted three times with ethyl acetate. The obtained organic layer was washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30 g, hexane/ethyl acetate=10/1). Thus, 1-(4-chloro-2-nitrophenyl)piperidine (471 mg, 96.4%) was yielded as an orange-colored oily material.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08816089B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-ee91ea45b0904751abc05dcff34d888c
Quellennotizuspto-grants-2014_08