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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 901103Erstellt: 24. Oktober 2026

1-Bromo-3-chloropropane → 5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/901103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-3-chloropropaneHCID 8006—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 5-hydroxy-1H-indole-2-carboxylateHCID 90677—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt5-(3-Chloro-propoxy)-1H-indole-2-carboxylic acid ethyl esterHCID 4511235674%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of ethyl-5-hydroxyindole-2-carboxylate (15 g, 73 mmol, 1.0 eq.) and 1-bromo-3-chloropropane (8.8 mL, 88 mmol, 1.2 eq.) in 2-butanone (200 mL) was added potassium carbonate (12.1 g, 88 mmol, 1.2 eq.). The reaction mixture was stirred 160 h at 80° C. The reaction mixture was cooled down and partitioned between ethyl acetate and water. The aqueous phase was extracted with ethyl acetate. The combined organic phases were washed with water and brine then dried over sodium sulfate, filtered and concentrated in vacuo. The crude mixture was purified by column chromatography on silica eluting with cyclohexane/ethyl acetate 9:1 to yield 15.3 mg (74%) of the title compound as a light yellow solid. MS (m/e): 282.7 (MH+, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07361682B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-891340eab47746c18ea2a6b9e9b1bd4d
Quellennotizuspto-grants-2008_04