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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 545083Erstellt: 26. Oktober 2026

Triethylamine → N,N-Bis-(4-methoxybenzyl)-(6-chloro-5-trifluoromethylpyridine-2-yl)amine

https://huagongshe.com/reaction/545083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBis(4-methoxybenzyl)amineHCID 714952—
Edukt2,6-Dichloro-3-(trifluoromethyl)pyridineHCID 1810337—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
ProduktN,N-Bis-(4-methoxybenzyl)-(6-chloro-5-trifluoromethylpyridine-2-yl)amineHCID 86605106—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Add bis(4-methoxybenzyl)amine (35.7 g, 138.9 mmol) in 20 mL of N-methylpyrrolidone to a solution of 2,6-dichloro-3-trifluoromethylpyridine (20 g, 92.6 mmol) and triethylamine (19.4 mL, 138.9 mmol) in 100 mL of N-methylpyrrolidone. Raise the temperature to 120° C., and stir the reaction for 14 hours. Quench the reaction mixture by the addition of water (80 mL), followed by extraction with EtOAc (3×70 mL). Wash the combined organic extracts with water (2×70 mL) and brine (70 mL), and dry over anhydrous Na2SO4. Filter the dried extract and concentrate under vacuum to afford the crude product, which is purified by column chromatography to give a yellow solid. 1H NMR (400 MHz, CDCl3) δ 7.58 (d, 1H, J=8.4 Hz), 7.15 (m, 4H), 6.85 (m, 4H), 6.31 (d, 1H, J=8.8 Hz), 4.70 (s, 4H), 3.80 (s, 6H). Mass spec. (436.99, M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07935702B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-3472bab536a54267a5eed4ab91871cf4
Quellennotizuspto-grants-2011_05