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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 415116Erstellt: 24. Oktober 2026

Diisopropylethylamine → Tert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/415116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3,4-DinitrofluorobenzeneHCID 298675—
Edukttert-Butyl 3-methylpiperazine-1-carboxylateHCID 2756810—
LösungsmittelDimethylacetamideHCID 31374—
ProduktTert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylateHCID 59349587—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

4-Fluoro-1,2-dinitrobenzene (0.93 g, 5.0 mmol, commercially available from Oakwood Products) and tert-butyl 3-methylpiperazine-1-carboxylate (1.0 g, 5.0 mmol) were dissolved in 3 mL of DMA, and 3 mL of diisopropylethylamine was added. The mixture was stirred at 50° C. overnight, and then cooled to room temperature, separated between ethyl acetate and water. The combined organic were washed with water, brine, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was separated by silica gel column (20% to 40% ethyl acetate in hexanes) to give 1.0 g of tert-butyl 4-(3,4-dinitrophenyl)-3-methylpiperazine-1-carboxylate. 1H-NMR (400 MHz, CDCl3): δ 8.05 (d, 2H), 6.84 (m, 2H), 3.90-4.10 (m, 3H), 3.05-3.60 (m, 4H), 1.50 (s, 9H), 1.10 (s, 3H). MS (EI): 367 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088767B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-db0ed36138b04b8ca6901f55354d3b4c
Quellennotizuspto-grants-2012_01