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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 876248Erstellt: 24. Oktober 2026

Triethylamine → 4-Nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylate

https://huagongshe.com/de/reaction/876248

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-Nitrophenyl chloroformateHCID 82129—
EduktSodium BicarbonateHCID 516892—
EduktN-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamideHCID 66701397—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Nitrophenyl 3-[(phenylcarbonyl)amino]-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxylateHCID 66701467—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

At 0° C., 1.5 g (4.3 mmol) of N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide and 1.2 ml (1.1 mmol) of triethylamine were initially charged in 131 ml of dichloromethane, and 868 mg (4.3 mmol) of 4-nitrophenyl chlorocarbonate were added slowly. The mixture was stirred at 0° C. for 2 h and then warmed to RT. Water and saturated aqueous sodium bicarbonate solution were added, and the reaction mixture was extracted. The organic phase was concentrated under reduced pressure and purified by column chromatography (cyclohexane/ethyl acetate 1:2). Yield: 1.95 g (88% of theory)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987248B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-5ad197d86fac4986b747e1ecf455f861
Quellennotizuspto-grants-2015_03