Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1764870Erstellt: 26. Oktober 2026

Indole → 1-(3-Chloropropyl)-1H-indole

https://huagongshe.com/reaction/1764870

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndoleHCID 798—
Edukt1-Bromo-3-chloropropaneHCID 8006—
EduktPotassium HydroxideHCID 14797—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-(3-Chloropropyl)-1H-indoleHCID 2204896071%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

To a solution of 1-bromo-3-chloropropane (2.00 g, 12.7 mmol) in DMF (7.0 mL) was added indole (500 mg, 4.24 mmol) followed by powdered KOH (262 mg, 4.66 mmol) at 20° C. The reaction mixture was then stirred for 15 h at 20° C. The reaction was quenched by addition of H2O and the product was extracted with Et2O. The organic solution was washed with H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. 1-(3-Chloro-1-propyl)indole (580 mg, 71%) was isolated by flash chromatography on a silica gel column by elution with EtOAc/Hexanes a pale yellow oil. 1H NMR (CDCl3, 300 MHz) δ2.28 (qu, 2H, J=6.3 Hz), 3.46 (t, 2H, J=6.2 Hz), 4.36 (t, 2H, J=6.6 Hz), 6.51 (d, 1H, J=3.3 Hz), 7.09-7.18 (m, 2H), 7.20-7.25 (m, 1H), 7.38 (d, 1H, J=8.5 Hz), 7.64 (d, 1H, J=7.7 Hz) ppm.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE039679E1
Quelldatensatzuspto-grants-2007_06
ORD IDord-ba1eb35f1598431183df44705ff2353b
Quellennotizuspto-grants-2007_06