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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40797Erstellt: 23. Oktober 2026

Potassium Iodide → 3-(Quinolin-4-yloxy)propan-1-ol

https://huagongshe.com/de/reaction/40797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPotassium CarbonateHCID 11430—
Edukt3-Chloro-1-propanolHCID 12313—
Eduktquinolin-4-olHCID 178516385—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(Quinolin-4-yloxy)propan-1-olHCID 6857625028%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A suspension of quinolin-4-ol (1.35 g, 9.30 mmol), anhydrous potassium carbonate (3.73 g, 26 mmol) and potassium iodide (4.23 g) in anhydrous DMF (8 mL) was stirred at 25° C. for 30 minutes. 3-Chloropropanol (2.93 g, 31 mmol) was added and the reaction was stirred until the starting material was consumed. The reaction was diluted with dichloromethane and extracted with water. The product was obtained as a slightly yellow solid (0.5298 g, 28%) after evaporation of the dichloromethane layer, and was used for the next step without further purification. 1H NMR (400 MHz, CDCl3): 2.09 (2H, m), 3.93 (2H, t, J=5.6 Hz), 4.10 (2H, t, J=5.6 Hz), 4.51 (11H, s), 6.25 (1H, d, J=5.5 Hz), 7.32 (1H, t, J=7.4 Hz), 7.56 (1H, t, J=8.2 Hz), 7.90 (1H, d, J=8.4 Hz), 7.93 (1H, d, J=8.4 Hz), 8.36 (1H, d, J=5.3 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530491B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-d91781c33a6f4b49b78e7d1ae719acf2
Quellennotizuspto-grants-2013_09